Canonical Allele Identifier: CA961070322
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1892931244

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431400C>A , CM000676.2:g.23431400C>A GRCh38
NC_000014.8:g.23900609C>A , CM000676.1:g.23900609C>A GRCh37
NC_000014.7:g.22970449C>A NCBI36
NG_007884.1:g.9262G>T , LRG_384:g.9262G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.796+18G>T MANE Select ENSP00000347507.3:n.796+18G>T
ENST00000355349.3:c.796+18G>T ENSP00000347507.3:n.796+18G>T
NM_000257.3:c.796+18G>T NP_000248.2:n.796+18G>T
XR_245686.3:n.902+18G>T
XM_017021340.1:c.796+18G>T XP_016876829.1:n.796+18G>T
NM_000257.4:c.796+18G>T MANE Select NP_000248.2:n.796+18G>T