Canonical Allele Identifier: CA384945629

Gene: KRT2

Linked Data

• MyVariant Identifiers: chr12:g.53045821A>G (hg19) ; chr12:g.52652037A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52652037A>G , CM000674.2:g.52652037A>G	GRCh38
NC_000012.11:g.53045821A>G , CM000674.1:g.53045821A>G	GRCh37
NC_000012.10:g.51332088A>G	NCBI36
NG_008296.1:g.5139T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309680.4:c.106T>C MANE Select	ENSP00000310861.3:p.Ser36Pro
ENST00000309680.3:c.106T>C	ENSP00000310861.3:p.Ser36Pro
NM_000423.2:c.106T>C	NP_000414.2:p.Ser36Pro
NM_000423.3:c.106T>C MANE Select	NP_000414.2:p.Ser36Pro