Canonical Allele Identifier: CA485622608
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1595081298
MyVariant Identifiers: chr14:g.23892834C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423625C>T , CM000676.2:g.23423625C>T GRCh38
NC_000014.8:g.23892834C>T , CM000676.1:g.23892834C>T GRCh37
NC_000014.7:g.22962674C>T NCBI36
NG_007884.1:g.17037G>A , LRG_384:g.17037G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3021G>A MANE Select ENSP00000347507.3:p.Leu1007=
ENST00000355349.3:c.3021G>A ENSP00000347507.3:p.Leu1007=
NM_000257.3:c.3021G>A NP_000248.2:p.Leu1007=
XR_245686.3:n.3127G>A
XM_017021340.1:c.3021G>A XP_016876829.1:p.Leu1007=
NM_000257.4:c.3021G>A MANE Select NP_000248.2:p.Leu1007=