Canonical Allele Identifier: CA2036598326
Gene: KRT2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52651842T= , CM000674.2:g.52651842T= GRCh38
NC_000012.11:g.53045626T= , CM000674.1:g.53045626T= GRCh37
NC_000012.10:g.51331893T= NCBI36
NG_008296.1:g.5334A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.301A= MANE Select ENSP00000310861.3:p.Ser101=
ENST00000309680.3:c.301A= ENSP00000310861.3:p.Ser101=
NM_000423.2:c.301A= NP_000414.2:p.Ser101=
NM_000423.3:c.301A= MANE Select NP_000414.2:p.Ser101=
Search 100 bp 5'
Search 100 bp 3'