Canonical Allele Identifier: CA6588838
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs745806170
ExAC: 12:53207724 C / T
gnomAD v2: 12-53207724-C-T
gnomAD v4: 12-52813940-C-T
MyVariant Identifiers: chr12:g.53207724C>T (hg19) chr12:g.52813940C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52813940C>T , CM000674.2:g.52813940C>T GRCh38
NC_000012.11:g.53207724C>T , CM000674.1:g.53207724C>T GRCh37
NC_000012.10:g.51493991C>T NCBI36
NG_007380.1:g.5612G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.119G>A MANE Select ENSP00000448220.1:p.Gly40Asp
ENST00000548097.5:c.119G>A ENSP00000449755.1:p.Gly40Asp
ENST00000551956.1:c.119G>A ENSP00000448220.1:p.Gly40Asp
ENST00000552668.1:c.119G>A ENSP00000447320.1:p.Gly40Asp
NM_002272.3:c.119G>A NP_002263.3:p.Gly40Asp
NM_002272.4:c.119G>A MANE Select NP_002263.3:p.Gly40Asp
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