Canonical Allele Identifier: CA384946670
Gene: KRT2 HGNC NCBI

Linked Data

gnomAD v4: 12-52652137-A-C
MyVariant Identifiers: chr12:g.53045921A>C (hg19) chr12:g.52652137A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652137A>C , CM000674.2:g.52652137A>C GRCh38
NC_000012.11:g.53045921A>C , CM000674.1:g.53045921A>C GRCh37
NC_000012.10:g.51332188A>C NCBI36
NG_008296.1:g.5039T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.6T>G MANE Select ENSP00000310861.3:p.Ser2Arg
ENST00000309680.3:c.6T>G ENSP00000310861.3:p.Ser2Arg
NM_000423.2:c.6T>G NP_000414.2:p.Ser2Arg
NM_000423.3:c.6T>G MANE Select NP_000414.2:p.Ser2Arg
Search 100 bp 5'
Search 100 bp 3'