Canonical Allele Identifier: CA2657074777

Gene: CYB5R3

Linked Data

• gnomAD v4: 22-42623646-G-GACGGGGCCACACCACCTGCCTCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623649_42623672dup , CM000684.2:g.42623649_42623672dup	GRCh38
NC_000022.10:g.43019655_43019678dup , CM000684.1:g.43019655_43019678dup	GRCh37
NC_000022.9:g.41349599_41349622dup	NCBI36
NG_012194.1:g.30730_30753dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.865+119_865+142dup	ENSP00000354468.5:n.865+119_865+142dup
ENST00000402438.6:c.664+119_664+142dup	ENSP00000385679.1:n.664+119_664+142dup
ENST00000407332.6:c.751+119_751+142dup	ENSP00000384457.2:n.751+119_751+142dup
ENST00000407623.8:c.664+119_664+142dup	ENSP00000384834.3:n.664+119_664+142dup
ENST00000617178.5:c.270+119_270+142dup
ENST00000684963.1:n.2473+119_2473+142dup
ENST00000685184.1:n.325+119_325+142dup
ENST00000686523.1:c.*682+119_*682+142dup	ENSP00000508940.1:n.*682+119_*682+142dup
ENST00000687183.1:n.1009+119_1009+142dup
ENST00000687198.1:c.664+119_664+142dup	ENSP00000508492.1:n.664+119_664+142dup
ENST00000688117.1:c.832+119_832+142dup	ENSP00000509015.1:n.832+119_832+142dup
ENST00000688244.1:c.433+119_433+142dup	ENSP00000510355.1:n.433+119_433+142dup
ENST00000689001.1:n.1355+119_1355+142dup
ENST00000689195.1:c.649+119_649+142dup	ENSP00000509895.1:n.649+119_649+142dup
ENST00000689239.1:n.900+119_900+142dup
ENST00000689795.1:n.994+119_994+142dup
ENST00000690835.1:c.*112+119_*112+142dup	ENSP00000509038.1:n.*112+119_*112+142dup
ENST00000690993.1:n.1488+119_1488+142dup
ENST00000691295.1:c.*216+119_*216+142dup	ENSP00000508706.1:n.*216+119_*216+142dup
ENST00000692152.1:c.664+119_664+142dup	ENSP00000509317.1:n.664+119_664+142dup
ENST00000692344.1:n.1220+119_1220+142dup
ENST00000693363.1:c.775+119_775+142dup	ENSP00000510411.1:n.775+119_775+142dup
ENST00000693367.1:c.733+119_733+142dup	ENSP00000508815.1:n.733+119_733+142dup
ENST00000352397.10:c.733+119_733+142dup MANE Select	ENSP00000338461.6:n.733+119_733+142dup
ENST00000352397.9:c.733+119_733+142dup	ENSP00000338461.6:n.733+119_733+142dup
ENST00000361740.8:c.832+119_832+142dup	ENSP00000354468.4:n.832+119_832+142dup
ENST00000402438.5:c.664+119_664+142dup	ENSP00000385679.1:n.664+119_664+142dup
ENST00000407332.5:c.664+119_664+142dup	ENSP00000384457.1:n.664+119_664+142dup
ENST00000407623.7:c.664+119_664+142dup	ENSP00000384834.3:n.664+119_664+142dup
ENST00000470741.1:n.2867+119_2867+142dup
NM_000398.6:c.733+119_733+142dup	NP_000389.1:n.733+119_733+142dup
NM_001129819.2:c.664+119_664+142dup	NP_001123291.1:n.664+119_664+142dup
NM_001171660.1:c.832+119_832+142dup	NP_001165131.1:n.832+119_832+142dup
NM_001171661.1:c.664+119_664+142dup	NP_001165132.1:n.664+119_664+142dup
NM_007326.4:c.664+119_664+142dup	NP_015565.1:n.664+119_664+142dup
NM_000398.7:c.733+119_733+142dup MANE Select	NP_000389.1:n.733+119_733+142dup
NM_001171660.2:c.832+119_832+142dup	NP_001165131.1:n.832+119_832+142dup