Canonical Allele Identifier: CA605088157
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1286423208
gnomAD v2: 12-53208063-A-G
gnomAD v4: 12-52814279-A-G
MyVariant Identifiers: chr12:g.53208063A>G (hg19) chr12:g.52814279A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814279A>G , CM000674.2:g.52814279A>G GRCh38
NC_000012.11:g.53208063A>G , CM000674.1:g.53208063A>G GRCh37
NC_000012.10:g.51494330A>G NCBI36
NG_007380.1:g.5273T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-221T>C ENSP00000448220.1:n.-221T>C
Search 100 bp 5'
Search 100 bp 3'