Canonical Allele Identifier: CA033786
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs748710204
ExAC: 14:23893928 A / G
gnomAD v2: 14-23893928-A-G
gnomAD v3: 14-23424719-A-G
gnomAD v4: 14-23424719-A-G
MyVariant Identifiers: chr14:g.23893928A>G (hg19) chr14:g.23424719A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424719A>G , CM000676.2:g.23424719A>G GRCh38
NC_000014.8:g.23893928A>G , CM000676.1:g.23893928A>G GRCh37
NC_000014.7:g.22963768A>G NCBI36
NG_007884.1:g.15943T>C , LRG_384:g.15943T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.2679+50T>C MANE Select ENSP00000347507.3:n.2679+50T>C
ENST00000355349.3:c.2679+50T>C ENSP00000347507.3:n.2679+50T>C
NM_000257.3:c.2679+50T>C NP_000248.2:n.2679+50T>C
XR_245686.3:n.2785+50T>C
XM_017021340.1:c.2679+50T>C XP_016876829.1:n.2679+50T>C
NM_000257.4:c.2679+50T>C MANE Select NP_000248.2:n.2679+50T>C
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