Canonical Allele Identifier: CA2617534639

Linked Data

gnomAD v4: 12-9115991-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115991T>C , CM000674.2:g.9115991T>C GRCh38
NC_000012.11:g.9268587T>C , CM000674.1:g.9268587T>C GRCh37
NC_000012.10:g.9159854T>C NCBI36
NG_011717.1:g.4972A>G
NG_011717.2:g.4972A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318602.11:c.-142A>G (A2M) ENSP00000323929.7:n.-142A>G
ENST00000404455.2:c.-17-125A>G (A2M) ENSP00000385710.2:n.-17-125A>G
ENST00000467091.1:n.71A>G (A2M)
ENST00000497324.1:n.27A>G (A2M)
NM_000014.5:c.-142A>G (A2M) NP_000005.2:n.-142A>G
NM_001347423.1:c.-17-125A>G (A2M) NP_001334352.1:n.-17-125A>G
NM_001347424.1:c.-595A>G (A2M) NP_001334353.1:n.-595A>G
NM_001347425.1:c.-432A>G (A2M) NP_001334354.1:n.-432A>G
XM_017018683.1:c.*34-9383T>C (KLRG1) XP_016874172.1:n.*34-9383T>C
XM_017018684.1:c.*34-19095T>C (KLRG1) XP_016874173.1:n.*34-19095T>C
XM_017018685.1:c.*33+57825T>C (KLRG1) XP_016874174.1:n.*33+57825T>C
NM_001347423.2:c.-17-125A>G (A2M) NP_001334352.2:n.-17-125A>G