Canonical Allele Identifier: CA466334555

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486232C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723950C>A , CM000671.2:g.91723950C>A	GRCh38
NC_000009.11:g.94486232C>A , CM000671.1:g.94486232C>A	GRCh37
NC_000009.10:g.93526053C>A	NCBI36
NG_008089.1:g.231213G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2544G>T MANE Select	ENSP00000364860.3:p.Pro848=
ENST00000375708.3:c.2544G>T	ENSP00000364860.3:p.Pro848=
ENST00000375715.5:c.1920+204G>T	ENSP00000364867.1:n.1920+204G>T
ENST00000550066.5:n.3012G>T
NM_004560.3:c.2544G>T	NP_004551.2:p.Pro848=
XM_005252008.3:c.2124G>T	XP_005252065.1:p.Pro708=
XM_005252009.3:c.1341G>T	XP_005252066.1:p.Pro447=
XM_006717121.2:c.2124G>T	XP_006717184.1:p.Pro708=
XM_011518721.1:c.2124G>T	XP_011517023.1:p.Pro708=
XM_005252008.4:c.2124G>T	XP_005252065.1:p.Pro708=
XM_006717121.3:c.2124G>T	XP_006717184.1:p.Pro708=
XM_017014762.1:c.2535G>T	XP_016870251.1:p.Pro845=
XM_017014763.1:c.2124G>T	XP_016870252.1:p.Pro708=
NM_004560.4:c.2544G>T MANE Select	NP_004551.2:p.Pro848=