Canonical Allele Identifier: CA2617534756

Linked Data

gnomAD v4: 12-9116089-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116089G>A , CM000674.2:g.9116089G>A GRCh38
NC_000012.11:g.9268685G>A , CM000674.1:g.9268685G>A GRCh37
NC_000012.10:g.9159952G>A NCBI36
NG_011717.1:g.4874C>T
NG_011717.2:g.4874C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-240C>T (A2M) ENSP00000323929.7:n.-240C>T
ENST00000404455.2:c.-18+39C>T (A2M) ENSP00000385710.2:n.-18+39C>T
NM_000014.5:c.-240C>T (A2M) NP_000005.2:n.-240C>T
NM_001347423.1:c.-18+39C>T (A2M) NP_001334352.1:n.-18+39C>T
NM_001347424.1:c.-693C>T (A2M) NP_001334353.1:n.-693C>T
NM_001347425.1:c.-530C>T (A2M) NP_001334354.1:n.-530C>T
XM_017018683.1:c.*34-9285G>A (KLRG1) XP_016874172.1:n.*34-9285G>A
XM_017018684.1:c.*34-18997G>A (KLRG1) XP_016874173.1:n.*34-18997G>A
XM_017018685.1:c.*33+57923G>A (KLRG1) XP_016874174.1:n.*33+57923G>A
NM_001347423.2:c.-18+39C>T (A2M) NP_001334352.2:n.-18+39C>T