Canonical Allele Identifier: CA473358297

Gene: CYP2R1

Linked Data

• MyVariant Identifiers: chr11:g.14900727A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14879181A>G , CM000673.2:g.14879181A>G	GRCh38
NC_000011.9:g.14900727A>G , CM000673.1:g.14900727A>G	GRCh37
NC_000011.8:g.14857303A>G	NCBI36
NG_007936.1:g.18025T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334636.10:c.1263T>C MANE Select	ENSP00000334592.5:p.His421=
ENST00000334636.9:c.1263T>C	ENSP00000334592.5:p.His421=
ENST00000525015.1:c.93T>C
ENST00000530609.5:c.*859T>C	ENSP00000466060.1:n.*859T>C
ENST00000532378.5:c.564T>C	ENSP00000435484.1:p.His188=
ENST00000532805.1:c.*371T>C	ENSP00000465097.1:n.*371T>C
ENST00000534686.5:c.*623T>C	ENSP00000432087.2:n.*623T>C
NM_024514.4:c.1263T>C	NP_078790.2:p.His421=
XM_005252788.1:c.1119T>C	XP_005252845.1:p.His373=
XM_005252789.2:c.1101T>C	XP_005252846.1:p.His367=
XM_005252791.3:c.918T>C	XP_005252848.1:p.His306=
XM_006718142.2:c.1218T>C	XP_006718205.1:p.His406=
XM_011519894.1:c.918T>C	XP_011518196.1:p.His306=
XM_011519895.1:c.918T>C	XP_011518197.1:p.His306=
XM_011519896.1:c.918T>C	XP_011518198.1:p.His306=
XM_011519897.1:c.918T>C	XP_011518199.1:p.His306=
XM_011519898.1:c.918T>C	XP_011518200.1:p.His306=
XR_242777.2:n.1080T>C
XM_005252788.2:c.1119T>C	XP_005252845.1:p.His373=
XM_005252789.3:c.1101T>C	XP_005252846.1:p.His367=
XM_011519895.2:c.918T>C	XP_011518197.1:p.His306=
XM_011519898.3:c.918T>C	XP_011518200.1:p.His306=
XM_017017190.2:c.1098T>C	XP_016872679.1:p.His366=
XM_017017191.2:c.918T>C	XP_016872680.1:p.His306=
XM_017017192.2:c.918T>C	XP_016872681.1:p.His306=
XM_017017193.2:c.918T>C	XP_016872682.1:p.His306=
XM_017017194.2:c.918T>C	XP_016872683.1:p.His306=
XM_024448345.1:c.1098T>C	XP_024304113.1:p.His366=
XM_024448346.1:c.918T>C	XP_024304114.1:p.His306=
XM_024448347.1:c.918T>C	XP_024304115.1:p.His306=
XM_024448348.1:c.918T>C	XP_024304116.1:p.His306=
XR_002957123.1:n.1043T>C
XR_002957124.1:n.1309T>C
XR_242777.3:n.1080T>C
NM_001377214.1:c.918T>C	NP_001364143.1:p.His306=
NM_001377215.1:c.918T>C	NP_001364144.1:p.His306=
NM_001377216.1:c.918T>C	NP_001364145.1:p.His306=
NM_001377217.1:c.1101T>C	NP_001364146.1:p.His367=
NM_001377227.1:c.918T>C	NP_001364156.1:p.His306=
NM_024514.5:c.1263T>C MANE Select	NP_078790.2:p.His421=
NM_001400558.1:c.918T>C	NP_001387487.1:p.His306=
NM_001400559.1:c.918T>C	NP_001387488.1:p.His306=
NM_001400560.1:c.918T>C	NP_001387489.1:p.His306=
NM_001400561.1:c.918T>C	NP_001387490.1:p.His306=
NM_001400562.1:c.564T>C	NP_001387491.1:p.His188=
NM_001400563.1:c.564T>C	NP_001387492.1:p.His188=
NM_001400564.1:c.564T>C	NP_001387493.1:p.His188=
NM_001400565.1:c.564T>C	NP_001387494.1:p.His188=
NM_001400566.1:c.285T>C	NP_001387495.1:p.His95=
NM_001400567.1:c.1119T>C	NP_001387496.1:p.His373=
NM_001400568.1:c.1218T>C	NP_001387497.1:p.His406=
NR_174512.1:n.1130T>C
NR_174513.1:n.979T>C
NR_174514.1:n.1354T>C
NR_174515.1:n.1763T>C
NR_174516.1:n.941T>C
NR_174517.1:n.477T>C
NR_174518.1:n.1574T>C
NR_174519.1:n.1321T>C
NR_174520.1:n.1112T>C
NR_174521.1:n.1612T>C
NR_174522.1:n.1110T>C
NR_174523.1:n.1521T>C