Canonical Allele Identifier: CA2575487031
Gene: MYH7 HGNC NCBI

Linked Data

gnomAD v4: 14-23428916-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23428916T>G , CM000676.2:g.23428916T>G GRCh38
NC_000014.8:g.23898125T>G , CM000676.1:g.23898125T>G GRCh37
NC_000014.7:g.22967965T>G NCBI36
NG_007884.1:g.11746A>C , LRG_384:g.11746A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1407+39A>C MANE Select ENSP00000347507.3:n.1407+39A>C
ENST00000355349.3:c.1407+39A>C ENSP00000347507.3:n.1407+39A>C
NM_000257.3:c.1407+39A>C NP_000248.2:n.1407+39A>C
XR_245686.3:n.1513+39A>C
XM_017021340.1:c.1407+39A>C XP_016876829.1:n.1407+39A>C
NM_000257.4:c.1407+39A>C MANE Select NP_000248.2:n.1407+39A>C
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