Canonical Allele Identifier: CA485766452
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23888813G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419604G>A , CM000676.2:g.23419604G>A GRCh38
NC_000014.8:g.23888813G>A , CM000676.1:g.23888813G>A GRCh37
NC_000014.7:g.22958653G>A NCBI36
NG_007884.1:g.21058C>T , LRG_384:g.21058C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3732C>T MANE Select ENSP00000347507.3:p.Asn1244=
ENST00000355349.3:c.3732C>T ENSP00000347507.3:p.Asn1244=
NM_000257.3:c.3732C>T NP_000248.2:p.Asn1244=
XM_017021340.1:c.3732C>T XP_016876829.1:p.Asn1244=
NM_000257.4:c.3732C>T MANE Select NP_000248.2:p.Asn1244=