Canonical Allele Identifier: CA374869782

Gene: CRB2

Linked Data

• MyVariant Identifiers: chr9:g.126139256A>C (hg19) ; chr9:g.123376977A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376977A>C , CM000671.2:g.123376977A>C	GRCh38
NC_000009.11:g.126139256A>C , CM000671.1:g.126139256A>C	GRCh37
NC_000009.10:g.125179077A>C	NCBI36
NG_051311.1:g.27913A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3773A>C MANE Select	ENSP00000362734.3:p.Tyr1258Ser
ENST00000373631.7:c.3773A>C	ENSP00000362734.3:p.Tyr1258Ser
ENST00000460253.1:c.2777A>C	ENSP00000435279.1:p.Tyr926Ser
NM_173689.6:c.3773A>C	NP_775960.4:p.Tyr1258Ser
NR_104603.1:n.2887A>C
XM_005251934.1:c.2777A>C	XP_005251991.1:p.Tyr926Ser
XM_011518556.1:c.3746A>C	XP_011516858.1:p.Tyr1249Ser
XM_011518557.1:c.3578A>C	XP_011516859.1:p.Tyr1193Ser
XM_011518558.1:c.3578A>C	XP_011516860.1:p.Tyr1193Ser
XM_005251934.3:c.2777A>C	XP_005251991.1:p.Tyr926Ser
XM_011518556.3:c.3746A>C	XP_011516858.1:p.Tyr1249Ser
XM_011518557.3:c.3578A>C	XP_011516859.1:p.Tyr1193Ser
XM_011518558.3:c.3578A>C	XP_011516860.1:p.Tyr1193Ser
NM_173689.7:c.3773A>C MANE Select	NP_775960.4:p.Tyr1258Ser
NR_104603.2:n.2887A>C