Canonical Allele Identifier: CA480072892
Gene: KRT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53045636T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52651852T>C , CM000674.2:g.52651852T>C GRCh38
NC_000012.11:g.53045636T>C , CM000674.1:g.53045636T>C GRCh37
NC_000012.10:g.51331903T>C NCBI36
NG_008296.1:g.5324A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.291A>G MANE Select ENSP00000310861.3:p.Gly97=
ENST00000309680.3:c.291A>G ENSP00000310861.3:p.Gly97=
NM_000423.2:c.291A>G NP_000414.2:p.Gly97=
NM_000423.3:c.291A>G MANE Select NP_000414.2:p.Gly97=
Search 100 bp 5'
Search 100 bp 3'