Canonical Allele Identifier: CA118321
Gene: KERA HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 6520
ClinVar RCV Id: RCV000006893
dbSNP Id: rs121917860

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055762G>A , CM000674.2:g.91055762G>A GRCh38
NC_000012.10:g.89973670G>A NCBI36
NC_000012.11:g.91449539G>A , CM000674.1:g.91449539G>A GRCh37
NG_021223.1:g.7593C>T , LRG_538:g.7593C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000266719.3:c.520C>T ENSP00000266719.3:p.Gln174Ter
NM_007035.3:c.520C>T , LRG_538t1:c.520C>T NP_008966.1:p.Gln174Ter
XM_011537781.1:c.520C>T XP_011536083.1:p.Gln174Ter