Canonical Allele Identifier: CA11991865
Gene: ADAMTS2 HGNC NCBI

Linked Data

dbSNP Id: rs469568

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.179236407A>C , CM000667.2:g.179236407A>C GRCh38
NC_000005.9:g.178663408A>C , CM000667.1:g.178663408A>C GRCh37
NC_000005.8:g.178596014A>C NCBI36
NG_023212.2:g.113922T>G
NG_023212.3:g.113922T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000698889.1:c.689-28692T>G ENSP00000514008.1:n.689-28692T>G
ENST00000251582.12:c.689-28692T>G MANE Select ENSP00000251582.7:n.689-28692T>G
ENST00000518335.3:c.689-28692T>G ENSP00000489888.2:n.689-28692T>G
ENST00000251582.11:c.689-28692T>G ENSP00000251582.7:n.689-28692T>G
ENST00000274609.5:c.689-28692T>G ENSP00000274609.5:n.689-28692T>G
NM_014244.4:c.689-28692T>G NP_055059.2:n.689-28692T>G
NM_021599.2:c.689-28692T>G NP_067610.1:n.689-28692T>G
NM_021599.3:c.689-28692T>G NP_067610.1:n.689-28692T>G
NM_014244.5:c.689-28692T>G MANE Select NP_055059.2:n.689-28692T>G
NM_021599.4:c.689-28692T>G NP_067610.1:n.689-28692T>G