Canonical Allele Identifier: CA485616075
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1194644513
gnomAD v2: 14-23882989-C-T
gnomAD v4: 14-23413780-C-T
MyVariant Identifiers: chr14:g.23882989C>T (hg19) chr14:g.23413780C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23413780C>T , CM000676.2:g.23413780C>T GRCh38
NC_000014.8:g.23882989C>T , CM000676.1:g.23882989C>T GRCh37
NC_000014.7:g.22952829C>T NCBI36
NG_007884.1:g.26882G>A , LRG_384:g.26882G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5769G>A MANE Select ENSP00000347507.3:p.Lys1923=
ENST00000355349.3:c.5769G>A ENSP00000347507.3:p.Lys1923=
NM_000257.3:c.5769G>A NP_000248.2:p.Lys1923=
XM_017021340.1:c.5769G>A XP_016876829.1:p.Lys1923=
NM_000257.4:c.5769G>A MANE Select NP_000248.2:p.Lys1923=
Search 100 bp 5'
Search 100 bp 3'