Canonical Allele Identifier: CA485767218
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23896882A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23427673A>G , CM000676.2:g.23427673A>G GRCh38
NC_000014.8:g.23896882A>G , CM000676.1:g.23896882A>G GRCh37
NC_000014.7:g.22966722A>G NCBI36
NG_007884.1:g.12989T>C , LRG_384:g.12989T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1800T>C MANE Select ENSP00000347507.3:p.Pro600=
ENST00000355349.3:c.1800T>C ENSP00000347507.3:p.Pro600=
NM_000257.3:c.1800T>C NP_000248.2:p.Pro600=
XR_245686.3:n.1906T>C
XM_017021340.1:c.1800T>C XP_016876829.1:p.Pro600=
NM_000257.4:c.1800T>C MANE Select NP_000248.2:p.Pro600=