Canonical Allele Identifier: CA2617534697

Linked Data

gnomAD v4: 12-9116036-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116036G>A , CM000674.2:g.9116036G>A GRCh38
NC_000012.11:g.9268632G>A , CM000674.1:g.9268632G>A GRCh37
NC_000012.10:g.9159899G>A NCBI36
NG_011717.1:g.4927C>T
NG_011717.2:g.4927C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-187C>T (A2M) ENSP00000323929.7:n.-187C>T
ENST00000404455.2:c.-18+92C>T (A2M) ENSP00000385710.2:n.-18+92C>T
ENST00000467091.1:n.26C>T (A2M)
NM_000014.5:c.-187C>T (A2M) NP_000005.2:n.-187C>T
NM_001347423.1:c.-18+92C>T (A2M) NP_001334352.1:n.-18+92C>T
NM_001347424.1:c.-640C>T (A2M) NP_001334353.1:n.-640C>T
NM_001347425.1:c.-477C>T (A2M) NP_001334354.1:n.-477C>T
XM_017018683.1:c.*34-9338G>A (KLRG1) XP_016874172.1:n.*34-9338G>A
XM_017018684.1:c.*34-19050G>A (KLRG1) XP_016874173.1:n.*34-19050G>A
XM_017018685.1:c.*33+57870G>A (KLRG1) XP_016874174.1:n.*33+57870G>A
NM_001347423.2:c.-18+92C>T (A2M) NP_001334352.2:n.-18+92C>T