Canonical Allele Identifier: CA046355
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs201586880
ExAC: 14:23901105 G / C
gnomAD v2: 14-23901105-G-C
gnomAD v3: 14-23431896-G-C
gnomAD v4: 14-23431896-G-C
MyVariant Identifiers: chr14:g.23901105G>C (hg19) chr14:g.23431896G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431896G>C , CM000676.2:g.23431896G>C GRCh38
NC_000014.8:g.23901105G>C , CM000676.1:g.23901105G>C GRCh37
NC_000014.7:g.22970945G>C NCBI36
NG_007884.1:g.8766C>G , LRG_384:g.8766C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.531-27C>G MANE Select ENSP00000347507.3:n.531-27C>G
ENST00000355349.3:c.531-27C>G ENSP00000347507.3:n.531-27C>G
NM_000257.3:c.531-27C>G NP_000248.2:n.531-27C>G
XR_245686.3:n.637-27C>G
XM_017021340.1:c.531-27C>G XP_016876829.1:n.531-27C>G
NM_000257.4:c.531-27C>G MANE Select NP_000248.2:n.531-27C>G
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