Canonical Allele Identifier: CA2499219606
Gene: CRB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.123363039_123363040delinsAT , CM000671.2:g.123363039_123363040delinsAT GRCh38
NC_000009.11:g.126125318_126125319delinsAT , CM000671.1:g.126125318_126125319delinsAT GRCh37
NC_000009.10:g.125165139_125165140delinsAT NCBI36
NG_051311.1:g.13975_13976delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000373631.8:c.269_270delinsAT MANE Select ENSP00000362734.3:p.Thr90Asn
ENST00000359999.7:c.269_270delinsAT ENSP00000353092.3:p.Thr90Asn
ENST00000373631.7:c.269_270delinsAT ENSP00000362734.3:p.Thr90Asn
NM_173689.6:c.269_270delinsAT NP_775960.4:p.Thr90Asn
XM_011518556.1:c.269_270delinsAT XP_011516858.1:p.Thr90Asn
XM_011518557.1:c.74_75delinsAT XP_011516859.1:p.Thr25Asn
XM_011518558.1:c.74_75delinsAT XP_011516860.1:p.Thr25Asn
XM_011518556.3:c.269_270delinsAT XP_011516858.1:p.Thr90Asn
XM_011518557.3:c.74_75delinsAT XP_011516859.1:p.Thr25Asn
XM_011518558.3:c.74_75delinsAT XP_011516860.1:p.Thr25Asn
NM_173689.7:c.269_270delinsAT MANE Select NP_775960.4:p.Thr90Asn