Canonical Allele Identifier: CA6588896
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1555180376
ExAC: 12:53207932 T / A
gnomAD v2: 12-53207932-T-A
gnomAD v4: 12-52814148-T-A
MyVariant Identifiers: chr12:g.53207932T>A (hg19) chr12:g.53207932_53207933delinsAC (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814148T>A , CM000674.2:g.52814148T>A GRCh38
NC_000012.11:g.53207932T>A , CM000674.1:g.53207932T>A GRCh37
NC_000012.10:g.51494199T>A NCBI36
NG_007380.1:g.5404A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-90A>T ENSP00000448220.1:n.-90A>T
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