Canonical Allele Identifier: CA384953208

Gene: KRT6A

Linked Data

• dbSNP Id: rs1938181577
• gnomAD v3: 12-52488095-C-G
• gnomAD v4: 12-52488095-C-G
• MyVariant Identifiers: chr12:g.52881879C>G (hg19) ; chr12:g.52488095C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52488095C>G , CM000674.2:g.52488095C>G	GRCh38
NC_000012.11:g.52881879C>G , CM000674.1:g.52881879C>G	GRCh37
NC_000012.10:g.51168146C>G	NCBI36
NG_008298.1:g.10303G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330722.7:c.1433G>C MANE Select	ENSP00000369317.3:p.Gly478Ala
ENST00000330722.6:c.1433G>C	ENSP00000369317.3:p.Gly478Ala
NM_005554.3:c.1433G>C	NP_005545.1:p.Gly478Ala
NM_005554.4:c.1433G>C MANE Select	NP_005545.1:p.Gly478Ala