Canonical Allele Identifier: CA384945976
Gene: KRT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53045860T>G (hg19) chr12:g.52652076T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652076T>G , CM000674.2:g.52652076T>G GRCh38
NC_000012.11:g.53045860T>G , CM000674.1:g.53045860T>G GRCh37
NC_000012.10:g.51332127T>G NCBI36
NG_008296.1:g.5100A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.67A>C MANE Select ENSP00000310861.3:p.Ser23Arg
ENST00000309680.3:c.67A>C ENSP00000310861.3:p.Ser23Arg
NM_000423.2:c.67A>C NP_000414.2:p.Ser23Arg
NM_000423.3:c.67A>C MANE Select NP_000414.2:p.Ser23Arg
Search 100 bp 5'
Search 100 bp 3'