Canonical Allele Identifier: CA237244321
Gene: KRT2 HGNC NCBI

Linked Data

dbSNP Id: rs908964735
gnomAD v2: 12-53045644-C-T
gnomAD v3: 12-52651860-C-T
gnomAD v4: 12-52651860-C-T
MyVariant Identifiers: chr12:g.53045644C>T (hg19) chr12:g.52651860C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52651860C>T , CM000674.2:g.52651860C>T GRCh38
NC_000012.11:g.53045644C>T , CM000674.1:g.53045644C>T GRCh37
NC_000012.10:g.51331911C>T NCBI36
NG_008296.1:g.5316G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.283G>A MANE Select ENSP00000310861.3:p.Gly95Ser
ENST00000309680.3:c.283G>A ENSP00000310861.3:p.Gly95Ser
NM_000423.2:c.283G>A NP_000414.2:p.Gly95Ser
NM_000423.3:c.283G>A MANE Select NP_000414.2:p.Gly95Ser
Search 100 bp 5'
Search 100 bp 3'