Canonical Allele Identifier: CA689835550
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs1360961650

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520399A>G , CM000674.2:g.52520399A>G GRCh38
NC_000012.11:g.52914183A>G , CM000674.1:g.52914183A>G GRCh37
NC_000012.10:g.51200450A>G NCBI36
NG_008297.1:g.5061T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.8:c.-103T>C ENSP00000252242.4:n.-103T>C
ENST00000546577.1:c.-15T>C ENSP00000449651.1:n.-15T>C
NM_000424.3:c.-103T>C NP_000415.2:n.-103T>C