Canonical Allele Identifier: CA304067162
Gene: GAMT HGNC NCBI

Linked Data

dbSNP Id: rs1029909106
MyVariant Identifiers: chr19:g.1401134C>G (hg19) chr19:g.1401135C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401135C>G , CM000681.2:g.1401135C>G GRCh38
NC_000019.9:g.1401134C>G , CM000681.1:g.1401134C>G GRCh37
NC_000019.8:g.1352134C>G NCBI36
NG_009785.1:g.5419G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.181+161G>C MANE Select ENSP00000252288.1:n.181+161G>C
ENST00000447102.8:c.181+161G>C ENSP00000403536.2:n.181+161G>C
ENST00000640762.1:c.112+230G>C ENSP00000492031.1:n.112+230G>C
ENST00000252288.6:c.181+161G>C ENSP00000252288.1:n.181+161G>C
ENST00000447102.7:c.181+161G>C ENSP00000403536.2:n.181+161G>C
NM_000156.5:c.181+161G>C NP_000147.1:n.181+161G>C
NM_138924.2:c.181+161G>C NP_620279.1:n.181+161G>C
NM_000156.6:c.181+161G>C MANE Select NP_000147.1:n.181+161G>C
NM_138924.3:c.181+161G>C NP_620279.1:n.181+161G>C
Search 100 bp 5'
Search 100 bp 3'