Canonical Allele Identifier: CA199643020

Gene: CRB2

Linked Data

• dbSNP Id: rs961589579
• gnomAD v2: 9-126139140-A-G
• gnomAD v4: 9-123376861-A-G
• MyVariant Identifiers: chr9:g.126139140A>G (hg19) ; chr9:g.123376861A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376861A>G , CM000671.2:g.123376861A>G	GRCh38
NC_000009.11:g.126139140A>G , CM000671.1:g.126139140A>G	GRCh37
NC_000009.10:g.125178961A>G	NCBI36
NG_051311.1:g.27797A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3657A>G MANE Select	ENSP00000362734.3:p.Pro1219=
ENST00000373631.7:c.3657A>G	ENSP00000362734.3:p.Pro1219=
ENST00000460253.1:c.2661A>G	ENSP00000435279.1:p.Pro887=
NM_173689.6:c.3657A>G	NP_775960.4:p.Pro1219=
NR_104603.1:n.2771A>G
XM_005251934.1:c.2661A>G	XP_005251991.1:p.Pro887=
XM_011518556.1:c.3630A>G	XP_011516858.1:p.Pro1210=
XM_011518557.1:c.3462A>G	XP_011516859.1:p.Pro1154=
XM_011518558.1:c.3462A>G	XP_011516860.1:p.Pro1154=
XM_005251934.3:c.2661A>G	XP_005251991.1:p.Pro887=
XM_011518556.3:c.3630A>G	XP_011516858.1:p.Pro1210=
XM_011518557.3:c.3462A>G	XP_011516859.1:p.Pro1154=
XM_011518558.3:c.3462A>G	XP_011516860.1:p.Pro1154=
NM_173689.7:c.3657A>G MANE Select	NP_775960.4:p.Pro1219=
NR_104603.2:n.2771A>G