Canonical Allele Identifier: CA480073014
Gene: KRT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53045900A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652116A>T , CM000674.2:g.52652116A>T GRCh38
NC_000012.11:g.53045900A>T , CM000674.1:g.53045900A>T GRCh37
NC_000012.10:g.51332167A>T NCBI36
NG_008296.1:g.5060T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.27T>A MANE Select ENSP00000310861.3:p.Ser9=
ENST00000309680.3:c.27T>A ENSP00000310861.3:p.Ser9=
NM_000423.2:c.27T>A NP_000414.2:p.Ser9=
NM_000423.3:c.27T>A MANE Select NP_000414.2:p.Ser9=
Search 100 bp 5'
Search 100 bp 3'