Canonical Allele Identifier: CA485617932
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1595075455
MyVariant Identifiers: chr14:g.23886874C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417665C>A , CM000676.2:g.23417665C>A GRCh38
NC_000014.8:g.23886874C>A , CM000676.1:g.23886874C>A GRCh37
NC_000014.7:g.22956714C>A NCBI36
NG_007884.1:g.22997G>T , LRG_384:g.22997G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4191G>T MANE Select ENSP00000347507.3:p.Leu1397=
ENST00000355349.3:c.4191G>T ENSP00000347507.3:p.Leu1397=
NM_000257.3:c.4191G>T NP_000248.2:p.Leu1397=
XM_017021340.1:c.4191G>T XP_016876829.1:p.Leu1397=
NM_000257.4:c.4191G>T MANE Select NP_000248.2:p.Leu1397=