Canonical Allele Identifier: CA605088164
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs900635042
gnomAD v2: 12-53208148-C-A
gnomAD v3: 12-52814364-C-A
gnomAD v4: 12-52814364-C-A
MyVariant Identifiers: chr12:g.53208148C>A (hg19) chr12:g.52814364C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814364C>A , CM000674.2:g.52814364C>A GRCh38
NC_000012.11:g.53208148C>A , CM000674.1:g.53208148C>A GRCh37
NC_000012.10:g.51494415C>A NCBI36
NG_007380.1:g.5188G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-306G>T ENSP00000448220.1:n.-306G>T
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