Canonical Allele Identifier: CA373793250

Gene: ROR2

Linked Data

• dbSNP Id: rs1305393719
• gnomAD v2: 9-94486068-T-A
• gnomAD v4: 9-91723786-T-A
• MyVariant Identifiers: chr9:g.94486068T>A (hg19) ; chr9:g.91723786T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723786T>A , CM000671.2:g.91723786T>A	GRCh38
NC_000009.11:g.94486068T>A , CM000671.1:g.94486068T>A	GRCh37
NC_000009.10:g.93525889T>A	NCBI36
NG_008089.1:g.231377A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2708A>T MANE Select	ENSP00000364860.3:p.Asp903Val
ENST00000375708.3:c.2708A>T	ENSP00000364860.3:p.Asp903Val
ENST00000375715.5:c.1920+368A>T	ENSP00000364867.1:n.1920+368A>T
ENST00000550066.5:n.3176A>T
NM_004560.3:c.2708A>T	NP_004551.2:p.Asp903Val
XM_005252008.3:c.2288A>T	XP_005252065.1:p.Asp763Val
XM_005252009.3:c.1505A>T	XP_005252066.1:p.Asp502Val
XM_006717121.2:c.2288A>T	XP_006717184.1:p.Asp763Val
XM_011518721.1:c.2288A>T	XP_011517023.1:p.Asp763Val
XM_005252008.4:c.2288A>T	XP_005252065.1:p.Asp763Val
XM_006717121.3:c.2288A>T	XP_006717184.1:p.Asp763Val
XM_017014762.1:c.2699A>T	XP_016870251.1:p.Asp900Val
XM_017014763.1:c.2288A>T	XP_016870252.1:p.Asp763Val
NM_004560.4:c.2708A>T MANE Select	NP_004551.2:p.Asp903Val