Canonical Allele Identifier: CA2575099328

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115929C>A , CM000674.2:g.9115929C>A GRCh38
NC_000012.11:g.9268525C>A , CM000674.1:g.9268525C>A GRCh37
NC_000012.10:g.9159792C>A NCBI36
NG_011717.1:g.5034G>T
NG_011717.2:g.5034G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-80G>T (A2M) ENSP00000323929.7:n.-80G>T
ENST00000404455.2:c.-17-63G>T (A2M) ENSP00000385710.2:n.-17-63G>T
ENST00000467091.1:n.133G>T (A2M)
ENST00000497324.1:n.89G>T (A2M)
NM_000014.4:c.-80G>T (A2M) NP_000005.2:n.-80G>T
XM_006719056.2:c.-80G>T (A2M) XP_006719119.1:n.-80G>T
NM_000014.5:c.-80G>T (A2M) NP_000005.2:n.-80G>T
NM_001347423.1:c.-17-63G>T (A2M) NP_001334352.1:n.-17-63G>T
NM_001347424.1:c.-533G>T (A2M) NP_001334353.1:n.-533G>T
NM_001347425.1:c.-370G>T (A2M) NP_001334354.1:n.-370G>T
XM_006719056.3:c.-80G>T (A2M) XP_006719119.1:n.-80G>T
XM_017018683.1:c.*34-9445C>A (KLRG1) XP_016874172.1:n.*34-9445C>A
XM_017018684.1:c.*34-19157C>A (KLRG1) XP_016874173.1:n.*34-19157C>A
XM_017018685.1:c.*33+57763C>A (KLRG1) XP_016874174.1:n.*33+57763C>A
NM_001347423.2:c.-17-63G>T (A2M) NP_001334352.2:n.-17-63G>T