Canonical Allele Identifier: CA480072858
Gene: KRT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53045824T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652040T>G , CM000674.2:g.52652040T>G GRCh38
NC_000012.11:g.53045824T>G , CM000674.1:g.53045824T>G GRCh37
NC_000012.10:g.51332091T>G NCBI36
NG_008296.1:g.5136A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.103A>C MANE Select ENSP00000310861.3:p.Arg35=
ENST00000309680.3:c.103A>C ENSP00000310861.3:p.Arg35=
NM_000423.2:c.103A>C NP_000414.2:p.Arg35=
NM_000423.3:c.103A>C MANE Select NP_000414.2:p.Arg35=
Search 100 bp 5'
Search 100 bp 3'