Canonical Allele Identifier: CA389053523
Community Standard Title: NM_000257.4(MYH7):c.206T>C (p.Val69Ala)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433223A>G , CM000676.2:g.23433223A>G GRCh38
NC_000014.8:g.23902432A>G , CM000676.1:g.23902432A>G GRCh37
NC_000014.7:g.22972272A>G NCBI36
NG_007884.1:g.7439T>C , LRG_384:g.7439T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.206T>C MANE Select NP_000248.2:p.Val69Ala
ENST00000355349.4:c.206T>C MANE Select ENSP00000347507.3:p.Val69Ala
NM_000257.3:c.206T>C NP_000248.2:p.Val69Ala
ENST00000355349.3:c.206T>C ENSP00000347507.3:p.Val69Ala
XM_017021340.1:c.206T>C XP_016876829.1:p.Val69Ala
XR_245686.3:n.312T>C