Canonical Allele Identifier: CA6588919
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs143824965
ExAC: 12:53208029 G / A
gnomAD v2: 12-53208029-G-A
gnomAD v3: 12-52814245-G-A
gnomAD v4: 12-52814245-G-A
COSMIC: COSM2151370
MyVariant Identifiers: chr12:g.53208029G>A (hg19) chr12:g.52814245G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814245G>A , CM000674.2:g.52814245G>A GRCh38
NC_000012.11:g.53208029G>A , CM000674.1:g.53208029G>A GRCh37
NC_000012.10:g.51494296G>A NCBI36
NG_007380.1:g.5307C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-187C>T ENSP00000448220.1:n.-187C>T
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