Canonical Allele Identifier: CA913722891
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs1364786574

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492570G>A , CM000674.2:g.52492570G>A GRCh38
NC_000012.11:g.52886354G>A , CM000674.1:g.52886354G>A GRCh37
NC_000012.10:g.51172621G>A NCBI36
NG_008298.1:g.5828C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.540+79C>T MANE Select ENSP00000369317.3:n.540+79C>T
ENST00000330722.6:c.540+79C>T ENSP00000369317.3:n.540+79C>T
ENST00000549898.5:n.61+79C>T
NM_005554.3:c.540+79C>T NP_005545.1:n.540+79C>T
NM_005554.4:c.540+79C>T MANE Select NP_005545.1:n.540+79C>T