Canonical Allele Identifier: CA613317779
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1479564209
gnomAD v2: 14-23900772-G-T
gnomAD v4: 14-23431563-G-T
MyVariant Identifiers: chr14:g.23900772G>T (hg19) chr14:g.23431563G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431563G>T , CM000676.2:g.23431563G>T GRCh38
NC_000014.8:g.23900772G>T , CM000676.1:g.23900772G>T GRCh37
NC_000014.7:g.22970612G>T NCBI36
NG_007884.1:g.9099C>A , LRG_384:g.9099C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.732+22C>A MANE Select ENSP00000347507.3:n.732+22C>A
ENST00000355349.3:c.732+22C>A ENSP00000347507.3:n.732+22C>A
NM_000257.3:c.732+22C>A NP_000248.2:n.732+22C>A
XR_245686.3:n.838+22C>A
XM_017021340.1:c.732+22C>A XP_016876829.1:n.732+22C>A
NM_000257.4:c.732+22C>A MANE Select NP_000248.2:n.732+22C>A
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