Canonical Allele Identifier: CA232699782

Linked Data

dbSNP Id: rs16918022
gnomAD v2: 12-9268549-C-T
gnomAD v3: 12-9115953-C-T
gnomAD v4: 12-9115953-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115953C>T , CM000674.2:g.9115953C>T GRCh38
NC_000012.11:g.9268549C>T , CM000674.1:g.9268549C>T GRCh37
NC_000012.10:g.9159816C>T NCBI36
NG_011717.1:g.5010G>A
NG_011717.2:g.5010G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-104G>A (A2M) ENSP00000323929.7:n.-104G>A
ENST00000404455.2:c.-17-87G>A (A2M) ENSP00000385710.2:n.-17-87G>A
ENST00000467091.1:n.109G>A (A2M)
ENST00000497324.1:n.65G>A (A2M)
NM_000014.4:c.-104G>A (A2M) NP_000005.2:n.-104G>A
NM_000014.5:c.-104G>A (A2M) NP_000005.2:n.-104G>A
NM_001347423.1:c.-17-87G>A (A2M) NP_001334352.1:n.-17-87G>A
NM_001347424.1:c.-557G>A (A2M) NP_001334353.1:n.-557G>A
NM_001347425.1:c.-394G>A (A2M) NP_001334354.1:n.-394G>A
XM_017018683.1:c.*34-9421C>T (KLRG1) XP_016874172.1:n.*34-9421C>T
XM_017018684.1:c.*34-19133C>T (KLRG1) XP_016874173.1:n.*34-19133C>T
XM_017018685.1:c.*33+57787C>T (KLRG1) XP_016874174.1:n.*33+57787C>T
NM_001347423.2:c.-17-87G>A (A2M) NP_001334352.2:n.-17-87G>A