Canonical Allele Identifier: CA2036520142

Gene: KRT6A

Linked Data

• dbSNP Id: rs1228985171

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52488052C>G , CM000674.2:g.52488052C>G	GRCh38
NC_000012.11:g.52881836C>G , CM000674.1:g.52881836C>G	GRCh37
NC_000012.10:g.51168103C>G	NCBI36
NG_008298.1:g.10346G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330722.7:c.1459+17G>C MANE Select	ENSP00000369317.3:n.1459+17G>C
ENST00000330722.6:c.1459+17G>C	ENSP00000369317.3:n.1459+17G>C
NM_005554.3:c.1459+17G>C	NP_005545.1:n.1459+17G>C
NM_005554.4:c.1459+17G>C MANE Select	NP_005545.1:n.1459+17G>C