Canonical Allele Identifier: CA344037336

Gene: CRB1

Linked Data

• gnomAD v4: 1-197427761-A-C
• MyVariant Identifiers: chr1:g.197396891A>C (hg19) ; chr1:g.197427761A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427761A>C , CM000663.2:g.197427761A>C	GRCh38
NC_000001.10:g.197396891A>C , CM000663.1:g.197396891A>C	GRCh37
NC_000001.9:g.195663514A>C	NCBI36
NG_008483.1:g.164484A>C
NG_008483.2:g.231300A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2436A>C MANE Select	ENSP00000356370.3:p.Gln812His
ENST00000638467.1:c.2436A>C	ENSP00000491102.1:p.Gln812His
ENST00000681519.1:c.1317A>C	ENSP00000505267.1:p.Gln439His
ENST00000367397.1:c.579A>C	ENSP00000356367.1:p.Gln193His
ENST00000367399.6:c.2100A>C	ENSP00000356369.2:p.Gln700His
ENST00000367400.7:c.2436A>C	ENSP00000356370.3:p.Gln812His
ENST00000480086.2:n.337A>C
ENST00000484075.5:c.2436A>C	ENSP00000433932.1:p.Gln812His
ENST00000535699.5:c.2229A>C	ENSP00000438786.1:p.Gln743His
ENST00000538660.5:c.2128+5805A>C	ENSP00000438091.1:n.2128+5805A>C
NM_001193640.1:c.2100A>C	NP_001180569.1:p.Gln700His
NM_001257965.1:c.2229A>C	NP_001244894.1:p.Gln743His
NM_001257966.1:c.2128+5805A>C	NP_001244895.1:n.2128+5805A>C
NM_201253.2:c.2436A>C	NP_957705.1:p.Gln812His
NR_047563.1:n.2437A>C
NR_047564.1:n.2645A>C
XM_011509365.1:c.2436A>C	XP_011507667.1:p.Gln812His
XM_011509366.1:c.2436A>C	XP_011507668.1:p.Gln812His
XM_011509367.1:c.2436A>C	XP_011507669.1:p.Gln812His
XM_011509368.1:c.1854A>C	XP_011507670.1:p.Gln618His
XM_011509369.1:c.879A>C	XP_011507671.1:p.Gln293His
XM_011509365.2:c.2436A>C	XP_011507667.1:p.Gln812His
XM_011509369.2:c.879A>C	XP_011507671.1:p.Gln293His
XM_017000851.1:c.1593A>C	XP_016856340.1:p.Gln531His
XM_017000852.1:c.2436A>C	XP_016856341.1:p.Gln812His
NM_201253.3:c.2436A>C MANE Select	NP_957705.1:p.Gln812His
NM_001193640.2:c.2100A>C	NP_001180569.1:p.Gln700His
NM_001257965.2:c.2229A>C	NP_001244894.1:p.Gln743His
NR_047563.2:n.2389A>C
NR_047564.2:n.2597A>C
NM_001257966.2:c.2128+5805A>C	NP_001244895.1:n.2128+5805A>C