Canonical Allele Identifier: CA374869597

Gene: CRB2

Linked Data

• MyVariant Identifiers: chr9:g.126139157T>C (hg19) ; chr9:g.123376878T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376878T>C , CM000671.2:g.123376878T>C	GRCh38
NC_000009.11:g.126139157T>C , CM000671.1:g.126139157T>C	GRCh37
NC_000009.10:g.125178978T>C	NCBI36
NG_051311.1:g.27814T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3674T>C MANE Select	ENSP00000362734.3:p.Val1225Ala
ENST00000373631.7:c.3674T>C	ENSP00000362734.3:p.Val1225Ala
ENST00000460253.1:c.2678T>C	ENSP00000435279.1:p.Val893Ala
NM_173689.6:c.3674T>C	NP_775960.4:p.Val1225Ala
NR_104603.1:n.2788T>C
XM_005251934.1:c.2678T>C	XP_005251991.1:p.Val893Ala
XM_011518556.1:c.3647T>C	XP_011516858.1:p.Val1216Ala
XM_011518557.1:c.3479T>C	XP_011516859.1:p.Val1160Ala
XM_011518558.1:c.3479T>C	XP_011516860.1:p.Val1160Ala
XM_005251934.3:c.2678T>C	XP_005251991.1:p.Val893Ala
XM_011518556.3:c.3647T>C	XP_011516858.1:p.Val1216Ala
XM_011518557.3:c.3479T>C	XP_011516859.1:p.Val1160Ala
XM_011518558.3:c.3479T>C	XP_011516860.1:p.Val1160Ala
NM_173689.7:c.3674T>C MANE Select	NP_775960.4:p.Val1225Ala
NR_104603.2:n.2788T>C