Canonical Allele Identifier: CA373799241

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94488823C>A (hg19) ; chr9:g.91726541C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726541C>A , CM000671.2:g.91726541C>A	GRCh38
NC_000009.11:g.94488823C>A , CM000671.1:g.94488823C>A	GRCh37
NC_000009.10:g.93528644C>A	NCBI36
NG_008089.1:g.228622G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1386G>T MANE Select	ENSP00000364860.3:p.Gln462His
ENST00000375708.3:c.1386G>T	ENSP00000364860.3:p.Gln462His
ENST00000375715.5:c.966G>T	ENSP00000364867.1:p.Gln322His
ENST00000550066.5:n.1854G>T
NM_004560.3:c.1386G>T	NP_004551.2:p.Gln462His
XM_005252008.3:c.966G>T	XP_005252065.1:p.Gln322His
XM_005252009.3:c.183G>T	XP_005252066.1:p.Gln61His
XM_006717121.2:c.966G>T	XP_006717184.1:p.Gln322His
XM_011518721.1:c.966G>T	XP_011517023.1:p.Gln322His
NM_001318204.1:c.*53G>T	NP_001305133.1:n.*53G>T
XM_005252008.4:c.966G>T	XP_005252065.1:p.Gln322His
XM_006717121.3:c.966G>T	XP_006717184.1:p.Gln322His
XM_017014762.1:c.1377G>T	XP_016870251.1:p.Gln459His
XM_017014763.1:c.966G>T	XP_016870252.1:p.Gln322His
XR_001746315.1:n.1595G>T
NM_004560.4:c.1386G>T MANE Select	NP_004551.2:p.Gln462His
NM_001318204.2:c.*53G>T	NP_001305133.1:n.*53G>T