Canonical Allele Identifier: CA389053544
Community Standard Title: NM_000257.4(MYH7):c.202-2A>T
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433229T>A , CM000676.2:g.23433229T>A GRCh38
NC_000014.8:g.23902438T>A , CM000676.1:g.23902438T>A GRCh37
NC_000014.7:g.22972278T>A NCBI36
NG_007884.1:g.7433A>T , LRG_384:g.7433A>T

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.202-2A>T MANE Select NP_000248.2:n.202-2A>T
ENST00000355349.4:c.202-2A>T MANE Select ENSP00000347507.3:n.202-2A>T
NM_000257.3:c.202-2A>T NP_000248.2:n.202-2A>T
ENST00000355349.3:c.202-2A>T ENSP00000347507.3:n.202-2A>T
XM_017021340.1:c.202-2A>T XP_016876829.1:n.202-2A>T
XR_245686.3:n.308-2A>T