Canonical Allele Identifier: CA237228968

Gene: KRT6A

Linked Data

• dbSNP Id: rs560641385
• gnomAD v3: 12-52488184-G-T
• gnomAD v4: 12-52488184-G-T
• MyVariant Identifiers: chr12:g.52881968G>T (hg19) ; chr12:g.52488184G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52488184G>T , CM000674.2:g.52488184G>T	GRCh38
NC_000012.11:g.52881968G>T , CM000674.1:g.52881968G>T	GRCh37
NC_000012.10:g.51168235G>T	NCBI36
NG_008298.1:g.10214C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330722.7:c.1425-81C>A MANE Select	ENSP00000369317.3:n.1425-81C>A
ENST00000330722.6:c.1425-81C>A	ENSP00000369317.3:n.1425-81C>A
NM_005554.3:c.1425-81C>A	NP_005545.1:n.1425-81C>A
NM_005554.4:c.1425-81C>A MANE Select	NP_005545.1:n.1425-81C>A