Canonical Allele Identifier: CA343413825

Gene: DDR2

Linked Data

• dbSNP Id: rs1057519789
• gnomAD v2: 1-162745497-A-G
• gnomAD v4: 1-162775707-A-G
• MyVariant Identifiers: chr1:g.162745497A>G (hg19) ; chr1:g.162775707A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.162775707A>G , CM000663.2:g.162775707A>G	GRCh38
NC_000001.10:g.162745497A>G , CM000663.1:g.162745497A>G	GRCh37
NC_000001.9:g.161012121A>G	NCBI36
NG_016290.1:g.148270A>G
NG_016290.2:g.149495A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367921.8:c.1912A>G MANE Select	ENSP00000356898.3:p.Ile638Val
ENST00000446985.6:c.1912A>G	ENSP00000400309.2:p.Ile638Val
ENST00000367921.7:c.1912A>G	ENSP00000356898.3:p.Ile638Val
ENST00000367922.7:c.1912A>G	ENSP00000356899.2:p.Ile638Val
NM_001014796.1:c.1912A>G	NP_001014796.1:p.Ile638Val
NM_006182.2:c.1912A>G	NP_006173.2:p.Ile638Val
XM_006711344.2:c.1912A>G	XP_006711407.1:p.Ile638Val
XM_011509586.1:c.1912A>G	XP_011507888.1:p.Ile638Val
XM_011509587.1:c.1912A>G	XP_011507889.1:p.Ile638Val
NM_001014796.2:c.1912A>G	NP_001014796.1:p.Ile638Val
NM_001354982.1:c.1912A>G	NP_001341911.1:p.Ile638Val
NM_001354983.1:c.1912A>G	NP_001341912.1:p.Ile638Val
NM_006182.3:c.1912A>G	NP_006173.2:p.Ile638Val
XM_011509587.2:c.1912A>G	XP_011507889.1:p.Ile638Val
NM_006182.4:c.1912A>G MANE Select	NP_006173.2:p.Ile638Val
NM_001014796.3:c.1912A>G	NP_001014796.1:p.Ile638Val
NM_001354982.2:c.1912A>G	NP_001341911.1:p.Ile638Val
NM_001354983.2:c.1912A>G	NP_001341912.1:p.Ile638Val