Canonical Allele Identifier: CA77534627

Gene: ROBO2

Linked Data

• ClinVar Variation Id: 901084
• ClinVar RCV Id: RCV001146746
• dbSNP Id: rs545392588
• gnomAD v2: 3-77698774-T-C
• gnomAD v3: 3-77649623-T-C
• gnomAD v4: 3-77649623-T-C
• MyVariant Identifiers: chr3:g.77698774T>C (hg19) ; chr3:g.77649623T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.77649623T>C , CM000665.2:g.77649623T>C	GRCh38
NC_000003.11:g.77698774T>C , CM000665.1:g.77698774T>C	GRCh37
NC_000003.10:g.77781464T>C	NCBI36
NG_027734.1:g.1747930T>C
NG_027734.2:g.1747930T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696593.1:c.*3568T>C MANE Select	ENSP00000512738.1:n.*3568T>C
ENST00000461745.5:c.*3568T>C	ENSP00000417164.1:n.*3568T>C
ENST00000614793.4:c.7321T>C	ENSP00000480344.1:n.7321T>C
NM_001128929.3:c.*3568T>C	NP_001122401.1:n.*3568T>C
NM_001290039.1:c.*3568T>C	NP_001276968.1:n.*3568T>C
NM_001290040.1:c.*3568T>C	NP_001276969.1:n.*3568T>C
NM_001290065.1:c.*3568T>C	NP_001276994.1:n.*3568T>C
NM_002942.4:c.*3568T>C	NP_002933.1:n.*3568T>C
XM_011533981.2:c.*3565T>C	XP_011532283.1:n.*3565T>C
XM_017006988.1:c.*3565T>C	XP_016862477.1:n.*3565T>C
XM_017006994.1:c.*3565T>C	XP_016862483.1:n.*3565T>C
XM_017006995.1:c.*3565T>C	XP_016862484.1:n.*3565T>C
XM_017006997.1:c.*3565T>C	XP_016862486.1:n.*3565T>C
XM_017006999.1:c.*3565T>C	XP_016862488.1:n.*3565T>C
XM_017007001.1:c.*3565T>C	XP_016862490.1:n.*3565T>C
XM_017007005.1:c.*3565T>C	XP_016862494.1:n.*3565T>C
NM_001290039.2:c.*3568T>C	NP_001276968.1:n.*3568T>C
NM_001290040.2:c.*3568T>C	NP_001276969.1:n.*3568T>C
NM_001290065.2:c.*3568T>C	NP_001276994.1:n.*3568T>C
NM_002942.5:c.*3568T>C	NP_002933.1:n.*3568T>C
NM_001378190.1:c.*3568T>C	NP_001365119.1:n.*3568T>C
NM_001378191.1:c.*3568T>C	NP_001365120.1:n.*3568T>C
NM_001378192.1:c.*3568T>C	NP_001365121.1:n.*3568T>C
NM_001378193.1:c.*3568T>C	NP_001365122.1:n.*3568T>C
NM_001378194.1:c.*3565T>C	NP_001365123.1:n.*3565T>C
NM_001378195.1:c.*3568T>C	NP_001365124.1:n.*3568T>C
NM_001378196.1:c.*3565T>C	NP_001365125.1:n.*3565T>C
NM_001378197.1:c.*3568T>C	NP_001365126.1:n.*3568T>C
NM_001378198.1:c.*3568T>C	NP_001365127.1:n.*3568T>C
NM_001378199.1:c.*3565T>C	NP_001365128.1:n.*3565T>C
NM_001378200.1:c.*3568T>C	NP_001365129.1:n.*3568T>C
NM_001378201.1:c.*3565T>C	NP_001365130.1:n.*3565T>C
NM_001378202.1:c.*3568T>C	NP_001365131.1:n.*3568T>C
NM_001378203.1:c.*3565T>C	NP_001365132.1:n.*3565T>C
NM_001394212.1:c.*3568T>C	NP_001381141.1:n.*3568T>C
NM_001394213.1:c.*3568T>C	NP_001381142.1:n.*3568T>C
NM_001394214.1:c.*3568T>C	NP_001381143.1:n.*3568T>C
NM_001395656.1:c.*3568T>C MANE Select	NP_001382585.1:n.*3568T>C
NM_001395657.1:c.*3565T>C	NP_001382586.1:n.*3565T>C