Canonical Allele Identifier: CA2624254062
Gene: MYH7 HGNC NCBI

Linked Data

gnomAD v4: 14-23433511-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433511T>C , CM000676.2:g.23433511T>C GRCh38
NC_000014.8:g.23902720T>C , CM000676.1:g.23902720T>C GRCh37
NC_000014.7:g.22972560T>C NCBI36
NG_007884.1:g.7151A>G , LRG_384:g.7151A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.201+21A>G MANE Select ENSP00000347507.3:n.201+21A>G
ENST00000355349.3:c.201+21A>G ENSP00000347507.3:n.201+21A>G
NM_000257.3:c.201+21A>G NP_000248.2:n.201+21A>G
XR_245686.3:n.307+21A>G
XM_017021340.1:c.201+21A>G XP_016876829.1:n.201+21A>G
NM_000257.4:c.201+21A>G MANE Select NP_000248.2:n.201+21A>G
Search 100 bp 5'
Search 100 bp 3'