Canonical Allele Identifier: CA2617534806

Linked Data

gnomAD v4: 12-9116132-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116132A>G , CM000674.2:g.9116132A>G GRCh38
NC_000012.11:g.9268728A>G , CM000674.1:g.9268728A>G GRCh37
NC_000012.10:g.9159995A>G NCBI36
NG_011717.1:g.4831T>C
NG_011717.2:g.4831T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-283T>C (A2M) ENSP00000323929.7:n.-283T>C
ENST00000404455.2:c.-22T>C (A2M) ENSP00000385710.2:n.-22T>C
NM_000014.5:c.-283T>C (A2M) NP_000005.2:n.-283T>C
NM_001347423.1:c.-22T>C (A2M) NP_001334352.1:n.-22T>C
NM_001347424.1:c.-736T>C (A2M) NP_001334353.1:n.-736T>C
NM_001347425.1:c.-573T>C (A2M) NP_001334354.1:n.-573T>C
XM_017018683.1:c.*34-9242A>G (KLRG1) XP_016874172.1:n.*34-9242A>G
XM_017018684.1:c.*34-18954A>G (KLRG1) XP_016874173.1:n.*34-18954A>G
XM_017018685.1:c.*33+57966A>G (KLRG1) XP_016874174.1:n.*33+57966A>G
NM_001347423.2:c.-22T>C (A2M) NP_001334352.2:n.-22T>C