Canonical Allele Identifier: CA919089620
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1555180385

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814207_52814208dup , CM000674.2:g.52814207_52814208dup GRCh38
NC_000012.11:g.53207991_53207992dup , CM000674.1:g.53207991_53207992dup GRCh37
NC_000012.10:g.51494258_51494259dup NCBI36
NG_007380.1:g.5345_5346dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-149_-148dup ENSP00000448220.1:n.-149_-148dup