Canonical Allele Identifier: CA2036598675
Gene: KRT2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652156A= , CM000674.2:g.52652156A= GRCh38
NC_000012.11:g.53045940A= , CM000674.1:g.53045940A= GRCh37
NC_000012.10:g.51332207A= NCBI36
NG_008296.1:g.5020T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.-14T= MANE Select ENSP00000310861.3:n.-14T=
ENST00000309680.3:c.-14T= ENSP00000310861.3:n.-14T=
NM_000423.2:c.-14T= NP_000414.2:n.-14T=
NM_000423.3:c.-14T= MANE Select NP_000414.2:n.-14T=
Search 100 bp 5'
Search 100 bp 3'