Canonical Allele Identifier: CA237228976

Gene: KRT6A

Linked Data

• dbSNP Id: rs532803404
• gnomAD v3: 12-52488212-G-A
• gnomAD v4: 12-52488212-G-A
• MyVariant Identifiers: chr12:g.52881996G>A (hg19) ; chr12:g.52488212G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52488212G>A , CM000674.2:g.52488212G>A	GRCh38
NC_000012.11:g.52881996G>A , CM000674.1:g.52881996G>A	GRCh37
NC_000012.10:g.51168263G>A	NCBI36
NG_008298.1:g.10186C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330722.7:c.1425-109C>T MANE Select	ENSP00000369317.3:n.1425-109C>T
ENST00000330722.6:c.1425-109C>T	ENSP00000369317.3:n.1425-109C>T
NM_005554.3:c.1425-109C>T	NP_005545.1:n.1425-109C>T
NM_005554.4:c.1425-109C>T MANE Select	NP_005545.1:n.1425-109C>T