Canonical Allele Identifier: CA986598561

Gene: TIMP2

Linked Data

• dbSNP Id: rs2069674542
• gnomAD v3: 17-78870747-A-C
• gnomAD v4: 17-78870747-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78870747A>C , CM000679.2:g.78870747A>C	GRCh38
NC_000017.10:g.76866829A>C , CM000679.1:g.76866829A>C	GRCh37
NC_000017.9:g.74378424A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586713.6:c.109+151T>G	ENSP00000465968.2:n.109+151T>G
ENST00000706922.1:c.109+151T>G	ENSP00000516642.1:n.109+151T>G
ENST00000706923.1:c.109+151T>G	ENSP00000516643.1:n.109+151T>G
ENST00000262768.11:c.340+151T>G MANE Select	ENSP00000262768.6:n.340+151T>G
ENST00000536189.6:c.109+151T>G	ENSP00000441724.1:n.109+151T>G
ENST00000585421.5:c.109+151T>G	ENSP00000467584.1:n.109+151T>G
ENST00000586057.5:c.109+151T>G	ENSP00000468296.1:n.109+151T>G
ENST00000592761.2:c.109+151T>G	ENSP00000464930.1:n.109+151T>G
NM_003255.4:c.340+151T>G	NP_003246.1:n.340+151T>G
NM_003255.5:c.340+151T>G MANE Select	NP_003246.1:n.340+151T>G