Canonical Allele Identifier: CA480073003
Gene: KRT2 HGNC NCBI

Linked Data

gnomAD v4: 12-52652110-T-C
MyVariant Identifiers: chr12:g.53045894T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652110T>C , CM000674.2:g.52652110T>C GRCh38
NC_000012.11:g.53045894T>C , CM000674.1:g.53045894T>C GRCh37
NC_000012.10:g.51332161T>C NCBI36
NG_008296.1:g.5066A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.33A>G MANE Select ENSP00000310861.3:p.Gly11=
ENST00000309680.3:c.33A>G ENSP00000310861.3:p.Gly11=
NM_000423.2:c.33A>G NP_000414.2:p.Gly11=
NM_000423.3:c.33A>G MANE Select NP_000414.2:p.Gly11=
Search 100 bp 5'
Search 100 bp 3'