Canonical Allele Identifier: CA384945620
Gene: KRT2 HGNC NCBI

Linked Data

COSMIC: COSM4755365
MyVariant Identifiers: chr12:g.53045820G>T (hg19) chr12:g.52652036G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652036G>T , CM000674.2:g.52652036G>T GRCh38
NC_000012.11:g.53045820G>T , CM000674.1:g.53045820G>T GRCh37
NC_000012.10:g.51332087G>T NCBI36
NG_008296.1:g.5140C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.107C>A MANE Select ENSP00000310861.3:p.Ser36Ter
ENST00000309680.3:c.107C>A ENSP00000310861.3:p.Ser36Ter
NM_000423.2:c.107C>A NP_000414.2:p.Ser36Ter
NM_000423.3:c.107C>A MANE Select NP_000414.2:p.Ser36Ter
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