Canonical Allele Identifier: CA2015347064

Linked Data

dbSNP Id: rs1939096504
gnomAD v4: 12-9116040-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116040G>A , CM000674.2:g.9116040G>A GRCh38
NC_000012.11:g.9268636G>A , CM000674.1:g.9268636G>A GRCh37
NC_000012.10:g.9159903G>A NCBI36
NG_011717.1:g.4923C>T
NG_011717.2:g.4923C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-191C>T (A2M) ENSP00000323929.7:n.-191C>T
ENST00000404455.2:c.-18+88C>T (A2M) ENSP00000385710.2:n.-18+88C>T
ENST00000467091.1:n.22C>T (A2M)
NM_000014.5:c.-191C>T (A2M) NP_000005.2:n.-191C>T
NM_001347423.1:c.-18+88C>T (A2M) NP_001334352.1:n.-18+88C>T
NM_001347424.1:c.-644C>T (A2M) NP_001334353.1:n.-644C>T
NM_001347425.1:c.-481C>T (A2M) NP_001334354.1:n.-481C>T
XM_017018683.1:c.*34-9334G>A (KLRG1) XP_016874172.1:n.*34-9334G>A
XM_017018684.1:c.*34-19046G>A (KLRG1) XP_016874173.1:n.*34-19046G>A
XM_017018685.1:c.*33+57874G>A (KLRG1) XP_016874174.1:n.*33+57874G>A
NM_001347423.2:c.-18+88C>T (A2M) NP_001334352.2:n.-18+88C>T