Canonical Allele Identifier: CA373793348

Gene: ROR2

Linked Data

• gnomAD v4: 9-91723834-G-A
• MyVariant Identifiers: chr9:g.94486116G>A (hg19) ; chr9:g.91723834G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723834G>A , CM000671.2:g.91723834G>A	GRCh38
NC_000009.11:g.94486116G>A , CM000671.1:g.94486116G>A	GRCh37
NC_000009.10:g.93525937G>A	NCBI36
NG_008089.1:g.231329C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2660C>T MANE Select	ENSP00000364860.3:p.Ala887Val
ENST00000375708.3:c.2660C>T	ENSP00000364860.3:p.Ala887Val
ENST00000375715.5:c.1920+320C>T	ENSP00000364867.1:n.1920+320C>T
ENST00000550066.5:n.3128C>T
NM_004560.3:c.2660C>T	NP_004551.2:p.Ala887Val
XM_005252008.3:c.2240C>T	XP_005252065.1:p.Ala747Val
XM_005252009.3:c.1457C>T	XP_005252066.1:p.Ala486Val
XM_006717121.2:c.2240C>T	XP_006717184.1:p.Ala747Val
XM_011518721.1:c.2240C>T	XP_011517023.1:p.Ala747Val
XM_005252008.4:c.2240C>T	XP_005252065.1:p.Ala747Val
XM_006717121.3:c.2240C>T	XP_006717184.1:p.Ala747Val
XM_017014762.1:c.2651C>T	XP_016870251.1:p.Ala884Val
XM_017014763.1:c.2240C>T	XP_016870252.1:p.Ala747Val
NM_004560.4:c.2660C>T MANE Select	NP_004551.2:p.Ala887Val