Canonical Allele Identifier: CA502131008

Gene: TIMP2

Linked Data

• gnomAD v4: 17-78870899-T-C
• MyVariant Identifiers: chr17:g.76866981T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78870899T>C , CM000679.2:g.78870899T>C	GRCh38
NC_000017.10:g.76866981T>C , CM000679.1:g.76866981T>C	GRCh37
NC_000017.9:g.74378576T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586713.6:c.108A>G	ENSP00000465968.2:p.Ala36=
ENST00000706922.1:c.108A>G	ENSP00000516642.1:p.Ala36=
ENST00000706923.1:c.108A>G	ENSP00000516643.1:p.Ala36=
ENST00000262768.11:c.339A>G MANE Select	ENSP00000262768.6:p.Ala113=
ENST00000536189.6:c.108A>G	ENSP00000441724.1:p.Ala36=
ENST00000585421.5:c.108A>G	ENSP00000467584.1:p.Ala36=
ENST00000586057.5:c.108A>G	ENSP00000468296.1:p.Ala36=
ENST00000592761.2:c.108A>G	ENSP00000464930.1:p.Ala36=
NM_003255.4:c.339A>G	NP_003246.1:p.Ala113=
NM_003255.5:c.339A>G MANE Select	NP_003246.1:p.Ala113=