Canonical Allele Identifier: CA027969
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs578110720

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23429195C>T , CM000676.2:g.23429195C>T GRCh38
NC_000014.8:g.23898404C>T , CM000676.1:g.23898404C>T GRCh37
NC_000014.7:g.22968244C>T NCBI36
NG_007884.1:g.11467G>A , LRG_384:g.11467G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1257+34G>A MANE Select ENSP00000347507.3:n.1257+34G>A
ENST00000355349.3:c.1257+34G>A ENSP00000347507.3:n.1257+34G>A
NM_000257.3:c.1257+34G>A NP_000248.2:n.1257+34G>A
XR_245686.3:n.1363+34G>A
XM_017021340.1:c.1257+34G>A XP_016876829.1:n.1257+34G>A
NM_000257.4:c.1257+34G>A MANE Select NP_000248.2:n.1257+34G>A