Canonical Allele Identifier: CA237228595
Gene: KRT6A HGNC NCBI

Linked Data

dbSNP Id: rs113369052

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52487957T>A , CM000674.2:g.52487957T>A GRCh38
NC_000012.11:g.52881741T>A , CM000674.1:g.52881741T>A GRCh37
NC_000012.10:g.51168008T>A NCBI36
NG_008298.1:g.10441A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000330722.7:c.1460-2A>T MANE Select ENSP00000369317.3:n.1460-2A>T
ENST00000330722.6:c.1460-2A>T ENSP00000369317.3:n.1460-2A>T
NM_005554.3:c.1460-2A>T NP_005545.1:n.1460-2A>T
NM_005554.4:c.1460-2A>T MANE Select NP_005545.1:n.1460-2A>T