Canonical Allele Identifier: CA2036598473
Gene: KRT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52651968C= , CM000674.2:g.52651968C= GRCh38
NC_000012.11:g.53045752C= , CM000674.1:g.53045752C= GRCh37
NC_000012.10:g.51332019C= NCBI36
NG_008296.1:g.5208G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.175G= MANE Select ENSP00000310861.3:p.Gly59=
ENST00000309680.3:c.175G= ENSP00000310861.3:p.Gly59=
NM_000423.2:c.175G= NP_000414.2:p.Gly59=
NM_000423.3:c.175G= MANE Select NP_000414.2:p.Gly59=