Canonical Allele Identifier: CA374869640

Gene: CRB2

Linked Data

• gnomAD v4: 9-123376902-G-A
• MyVariant Identifiers: chr9:g.126139181G>A (hg19) ; chr9:g.123376902G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376902G>A , CM000671.2:g.123376902G>A	GRCh38
NC_000009.11:g.126139181G>A , CM000671.1:g.126139181G>A	GRCh37
NC_000009.10:g.125179002G>A	NCBI36
NG_051311.1:g.27838G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3698G>A MANE Select	ENSP00000362734.3:p.Cys1233Tyr
ENST00000373631.7:c.3698G>A	ENSP00000362734.3:p.Cys1233Tyr
ENST00000460253.1:c.2702G>A	ENSP00000435279.1:p.Cys901Tyr
NM_173689.6:c.3698G>A	NP_775960.4:p.Cys1233Tyr
NR_104603.1:n.2812G>A
XM_005251934.1:c.2702G>A	XP_005251991.1:p.Cys901Tyr
XM_011518556.1:c.3671G>A	XP_011516858.1:p.Cys1224Tyr
XM_011518557.1:c.3503G>A	XP_011516859.1:p.Cys1168Tyr
XM_011518558.1:c.3503G>A	XP_011516860.1:p.Cys1168Tyr
XM_005251934.3:c.2702G>A	XP_005251991.1:p.Cys901Tyr
XM_011518556.3:c.3671G>A	XP_011516858.1:p.Cys1224Tyr
XM_011518557.3:c.3503G>A	XP_011516859.1:p.Cys1168Tyr
XM_011518558.3:c.3503G>A	XP_011516860.1:p.Cys1168Tyr
NM_173689.7:c.3698G>A MANE Select	NP_775960.4:p.Cys1233Tyr
NR_104603.2:n.2812G>A