Canonical Allele Identifier: CA6585968

Gene: KRT2

Linked Data

• dbSNP Id: rs375327233
• ExAC: 12:53045826 C / T
• gnomAD v2: 12-53045826-C-T
• gnomAD v3: 12-52652042-C-T
• gnomAD v4: 12-52652042-C-T
• COSMIC: COSM4042907
• MyVariant Identifiers: chr12:g.53045826C>T (hg19) ; chr12:g.52652042C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52652042C>T , CM000674.2:g.52652042C>T	GRCh38
NC_000012.11:g.53045826C>T , CM000674.1:g.53045826C>T	GRCh37
NC_000012.10:g.51332093C>T	NCBI36
NG_008296.1:g.5134G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309680.4:c.101G>A MANE Select	ENSP00000310861.3:p.Arg34Gln
ENST00000309680.3:c.101G>A	ENSP00000310861.3:p.Arg34Gln
NM_000423.2:c.101G>A	NP_000414.2:p.Arg34Gln
NM_000423.3:c.101G>A MANE Select	NP_000414.2:p.Arg34Gln