Canonical Allele Identifier: CA1877945579

Gene: CRB2

Linked Data

• dbSNP Id: rs910152624

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376509C>T , CM000671.2:g.123376509C>T	GRCh38
NC_000009.11:g.126138788C>T , CM000671.1:g.126138788C>T	GRCh37
NC_000009.10:g.125178609C>T	NCBI36
NG_051311.1:g.27445C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3634-329C>T MANE Select	ENSP00000362734.3:n.3634-329C>T
ENST00000373631.7:c.3634-329C>T	ENSP00000362734.3:n.3634-329C>T
ENST00000460253.1:c.2638-329C>T	ENSP00000435279.1:n.2638-329C>T
NM_173689.6:c.3634-329C>T	NP_775960.4:n.3634-329C>T
NR_104603.1:n.2748-329C>T
XM_005251934.1:c.2638-329C>T	XP_005251991.1:n.2638-329C>T
XM_011518556.1:c.3607-329C>T	XP_011516858.1:n.3607-329C>T
XM_011518557.1:c.3439-329C>T	XP_011516859.1:n.3439-329C>T
XM_011518558.1:c.3439-329C>T	XP_011516860.1:n.3439-329C>T
XM_005251934.3:c.2638-329C>T	XP_005251991.1:n.2638-329C>T
XM_011518556.3:c.3607-329C>T	XP_011516858.1:n.3607-329C>T
XM_011518557.3:c.3439-329C>T	XP_011516859.1:n.3439-329C>T
XM_011518558.3:c.3439-329C>T	XP_011516860.1:n.3439-329C>T
NM_173689.7:c.3634-329C>T MANE Select	NP_775960.4:n.3634-329C>T
NR_104603.2:n.2748-329C>T