Canonical Allele Identifier: CA480073189
Gene: KRT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53045771G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52651987G>C , CM000674.2:g.52651987G>C GRCh38
NC_000012.11:g.53045771G>C , CM000674.1:g.53045771G>C GRCh37
NC_000012.10:g.51332038G>C NCBI36
NG_008296.1:g.5189C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.156C>G MANE Select ENSP00000310861.3:p.Gly52=
ENST00000309680.3:c.156C>G ENSP00000310861.3:p.Gly52=
NM_000423.2:c.156C>G NP_000414.2:p.Gly52=
NM_000423.3:c.156C>G MANE Select NP_000414.2:p.Gly52=
Search 100 bp 5'
Search 100 bp 3'