Canonical Allele Identifier: CA467206751

Gene: CRB2

Linked Data

• dbSNP Id: rs757129632
• MyVariant Identifiers: chr9:g.126136077G>C (hg19) ; chr9:g.123373798G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123373798G>C , CM000671.2:g.123373798G>C	GRCh38
NC_000009.11:g.126136077G>C , CM000671.1:g.126136077G>C	GRCh37
NC_000009.10:g.125175898G>C	NCBI36
NG_051311.1:g.24734G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3267G>C MANE Select	ENSP00000362734.3:p.Pro1089=
ENST00000359999.7:c.3267G>C	ENSP00000353092.3:p.Pro1089=
ENST00000373631.7:c.3267G>C	ENSP00000362734.3:p.Pro1089=
ENST00000460253.1:c.2271G>C	ENSP00000435279.1:p.Pro757=
NM_173689.6:c.3267G>C	NP_775960.4:p.Pro1089=
NR_104603.1:n.2381G>C
XM_005251934.1:c.2271G>C	XP_005251991.1:p.Pro757=
XM_011518556.1:c.3240G>C	XP_011516858.1:p.Pro1080=
XM_011518557.1:c.3072G>C	XP_011516859.1:p.Pro1024=
XM_011518558.1:c.3072G>C	XP_011516860.1:p.Pro1024=
XM_005251934.3:c.2271G>C	XP_005251991.1:p.Pro757=
XM_011518556.3:c.3240G>C	XP_011516858.1:p.Pro1080=
XM_011518557.3:c.3072G>C	XP_011516859.1:p.Pro1024=
XM_011518558.3:c.3072G>C	XP_011516860.1:p.Pro1024=
NM_173689.7:c.3267G>C MANE Select	NP_775960.4:p.Pro1089=
NR_104603.2:n.2381G>C