Canonical Allele Identifier: CA2575504373
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422157G>C , CM000676.2:g.23422157G>C GRCh38
NC_000014.8:g.23891366G>C , CM000676.1:g.23891366G>C GRCh37
NC_000014.7:g.22961206G>C NCBI36
NG_007884.1:g.18505C>G , LRG_384:g.18505C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3245+23C>G MANE Select ENSP00000347507.3:n.3245+23C>G
ENST00000355349.3:c.3245+23C>G ENSP00000347507.3:n.3245+23C>G
NM_000257.3:c.3245+23C>G NP_000248.2:n.3245+23C>G
XR_245686.3:n.3351+23C>G
XM_017021340.1:c.3245+23C>G XP_016876829.1:n.3245+23C>G
NM_000257.4:c.3245+23C>G MANE Select NP_000248.2:n.3245+23C>G