Canonical Allele Identifier: CA689878162
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs537631692
gnomAD v3: 12-52814415-G-C
gnomAD v4: 12-52814415-G-C
MyVariant Identifiers: chr12:g.53208199G>C (hg19) chr12:g.52814415G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814415G>C , CM000674.2:g.52814415G>C GRCh38
NC_000012.11:g.53208199G>C , CM000674.1:g.53208199G>C GRCh37
NC_000012.10:g.51494466G>C NCBI36
NG_007380.1:g.5137C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-357C>G ENSP00000448220.1:n.-357C>G
Search 100 bp 5'
Search 100 bp 3'