Canonical Allele Identifier: CA373793194

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486042C>G (hg19) ; chr9:g.91723760C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723760C>G , CM000671.2:g.91723760C>G	GRCh38
NC_000009.11:g.94486042C>G , CM000671.1:g.94486042C>G	GRCh37
NC_000009.10:g.93525863C>G	NCBI36
NG_008089.1:g.231403G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2734G>C MANE Select	ENSP00000364860.3:p.Ala912Pro
ENST00000375708.3:c.2734G>C	ENSP00000364860.3:p.Ala912Pro
ENST00000375715.5:c.1920+394G>C	ENSP00000364867.1:n.1920+394G>C
ENST00000550066.5:n.3202G>C
NM_004560.3:c.2734G>C	NP_004551.2:p.Ala912Pro
XM_005252008.3:c.2314G>C	XP_005252065.1:p.Ala772Pro
XM_005252009.3:c.1531G>C	XP_005252066.1:p.Ala511Pro
XM_006717121.2:c.2314G>C	XP_006717184.1:p.Ala772Pro
XM_011518721.1:c.2314G>C	XP_011517023.1:p.Ala772Pro
XM_005252008.4:c.2314G>C	XP_005252065.1:p.Ala772Pro
XM_006717121.3:c.2314G>C	XP_006717184.1:p.Ala772Pro
XM_017014762.1:c.2725G>C	XP_016870251.1:p.Ala909Pro
XM_017014763.1:c.2314G>C	XP_016870252.1:p.Ala772Pro
NM_004560.4:c.2734G>C MANE Select	NP_004551.2:p.Ala912Pro