Canonical Allele Identifier: CA2640201674
Gene: TIMP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78870846A>G , CM000679.2:g.78870846A>G GRCh38
NC_000017.10:g.76866928A>G , CM000679.1:g.76866928A>G GRCh37
NC_000017.9:g.74378523A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000586713.6:c.109+52T>C ENSP00000465968.2:n.109+52T>C
ENST00000706922.1:c.109+52T>C ENSP00000516642.1:n.109+52T>C
ENST00000706923.1:c.109+52T>C ENSP00000516643.1:n.109+52T>C
ENST00000262768.11:c.340+52T>C MANE Select ENSP00000262768.6:n.340+52T>C
ENST00000536189.6:c.109+52T>C ENSP00000441724.1:n.109+52T>C
ENST00000585421.5:c.109+52T>C ENSP00000467584.1:n.109+52T>C
ENST00000586057.5:c.109+52T>C ENSP00000468296.1:n.109+52T>C
ENST00000592761.2:c.109+52T>C ENSP00000464930.1:n.109+52T>C
NM_003255.4:c.340+52T>C NP_003246.1:n.340+52T>C
NM_003255.5:c.340+52T>C MANE Select NP_003246.1:n.340+52T>C