Canonical Allele Identifier: CA032656
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs200342157
ExAC: 14:23894464 G / A
gnomAD v2: 14-23894464-G-A
gnomAD v3: 14-23425255-G-A
gnomAD v4: 14-23425255-G-A
MyVariant Identifiers: chr14:g.23894464G>A (hg19) chr14:g.23425255G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23425255G>A , CM000676.2:g.23425255G>A GRCh38
NC_000014.8:g.23894464G>A , CM000676.1:g.23894464G>A GRCh37
NC_000014.7:g.22964304G>A NCBI36
NG_007884.1:g.15407C>T , LRG_384:g.15407C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2423+27C>T MANE Select ENSP00000347507.3:n.2423+27C>T
ENST00000355349.3:c.2423+27C>T ENSP00000347507.3:n.2423+27C>T
NM_000257.3:c.2423+27C>T NP_000248.2:n.2423+27C>T
XR_245686.3:n.2529+27C>T
XM_017021340.1:c.2423+27C>T XP_016876829.1:n.2423+27C>T
NM_000257.4:c.2423+27C>T MANE Select NP_000248.2:n.2423+27C>T
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