Canonical Allele Identifier: CA2123468932

Linked Data

dbSNP Id: rs143650929

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417430G>C , CM000676.2:g.23417430G>C GRCh38
NC_000014.8:g.23886639G>C , CM000676.1:g.23886639G>C GRCh37
NC_000014.7:g.22956479G>C NCBI36
NG_007884.1:g.23232C>G , LRG_384:g.23232C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4353+73C>G (MYH7) MANE Select ENSP00000347507.3:n.4353+73C>G
ENST00000355349.3:c.4353+73C>G (MYH7) ENSP00000347507.3:n.4353+73C>G
NM_000257.3:c.4353+73C>G (MYH7) NP_000248.2:n.4353+73C>G
NR_126491.1:n.813+57G>C (MHRT)
XM_017021340.1:c.4353+73C>G (MYH7) XP_016876829.1:n.4353+73C>G
NM_000257.4:c.4353+73C>G (MYH7) MANE Select NP_000248.2:n.4353+73C>G