Canonical Allele Identifier: CA2579446756

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377103T>C , CM000671.2:g.123377103T>C	GRCh38
NC_000009.11:g.126139382T>C , CM000671.1:g.126139382T>C	GRCh37
NC_000009.10:g.125179203T>C	NCBI36
NG_051311.1:g.28039T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.*41T>C MANE Select	ENSP00000362734.3:n.*41T>C
ENST00000373631.7:c.*41T>C	ENSP00000362734.3:n.*41T>C
ENST00000460253.1:c.*41T>C	ENSP00000435279.1:n.*41T>C
NM_173689.6:c.*41T>C	NP_775960.4:n.*41T>C
NR_104603.1:n.3013T>C
XM_005251934.1:c.*41T>C	XP_005251991.1:n.*41T>C
XM_011518556.1:c.*41T>C	XP_011516858.1:n.*41T>C
XM_011518557.1:c.*41T>C	XP_011516859.1:n.*41T>C
XM_011518558.1:c.*41T>C	XP_011516860.1:n.*41T>C
XM_005251934.3:c.*41T>C	XP_005251991.1:n.*41T>C
XM_011518556.3:c.*41T>C	XP_011516858.1:n.*41T>C
XM_011518557.3:c.*41T>C	XP_011516859.1:n.*41T>C
XM_011518558.3:c.*41T>C	XP_011516860.1:n.*41T>C
NM_173689.7:c.*41T>C MANE Select	NP_775960.4:n.*41T>C
NR_104603.2:n.3013T>C