Canonical Allele Identifier: CA2123453758
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1595081548

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423866C>G , CM000676.2:g.23423866C>G GRCh38
NC_000014.8:g.23893075C>G , CM000676.1:g.23893075C>G GRCh37
NC_000014.7:g.22962915C>G NCBI36
NG_007884.1:g.16796G>C , LRG_384:g.16796G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2922+41G>C MANE Select ENSP00000347507.3:n.2922+41G>C
ENST00000355349.3:c.2922+41G>C ENSP00000347507.3:n.2922+41G>C
NM_000257.3:c.2922+41G>C NP_000248.2:n.2922+41G>C
XR_245686.3:n.3028+41G>C
XM_017021340.1:c.2922+41G>C XP_016876829.1:n.2922+41G>C
NM_000257.4:c.2922+41G>C MANE Select NP_000248.2:n.2922+41G>C