Canonical Allele Identifier: CA237234723
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs569553196

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52492579G>A , CM000674.2:g.52492579G>A GRCh38
NC_000012.11:g.52886363G>A , CM000674.1:g.52886363G>A GRCh37
NC_000012.10:g.51172630G>A NCBI36
NG_008298.1:g.5819C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.540+70C>T MANE Select ENSP00000369317.3:n.540+70C>T
ENST00000330722.6:c.540+70C>T ENSP00000369317.3:n.540+70C>T
ENST00000549898.5:n.61+70C>T
NM_005554.3:c.540+70C>T NP_005545.1:n.540+70C>T
NM_005554.4:c.540+70C>T MANE Select NP_005545.1:n.540+70C>T