Canonical Allele Identifier: CA2618946587
Gene: KRT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652161G>T , CM000674.2:g.52652161G>T GRCh38
NC_000012.11:g.53045945G>T , CM000674.1:g.53045945G>T GRCh37
NC_000012.10:g.51332212G>T NCBI36
NG_008296.1:g.5015C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.-19C>A MANE Select ENSP00000310861.3:n.-19C>A
ENST00000309680.3:c.-19C>A ENSP00000310861.3:n.-19C>A
NM_000423.2:c.-19C>A NP_000414.2:n.-19C>A
NM_000423.3:c.-19C>A MANE Select NP_000414.2:n.-19C>A