Canonical Allele Identifier: CA2617534664

Linked Data

gnomAD v4: 12-9116008-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116008T>A , CM000674.2:g.9116008T>A GRCh38
NC_000012.11:g.9268604T>A , CM000674.1:g.9268604T>A GRCh37
NC_000012.10:g.9159871T>A NCBI36
NG_011717.1:g.4955A>T
NG_011717.2:g.4955A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000318602.11:c.-159A>T (A2M) ENSP00000323929.7:n.-159A>T
ENST00000404455.2:c.-18+120A>T (A2M) ENSP00000385710.2:n.-18+120A>T
ENST00000467091.1:n.54A>T (A2M)
ENST00000497324.1:n.10A>T (A2M)
NM_000014.5:c.-159A>T (A2M) NP_000005.2:n.-159A>T
NM_001347423.1:c.-18+120A>T (A2M) NP_001334352.1:n.-18+120A>T
NM_001347424.1:c.-612A>T (A2M) NP_001334353.1:n.-612A>T
NM_001347425.1:c.-449A>T (A2M) NP_001334354.1:n.-449A>T
XM_017018683.1:c.*34-9366T>A (KLRG1) XP_016874172.1:n.*34-9366T>A
XM_017018684.1:c.*34-19078T>A (KLRG1) XP_016874173.1:n.*34-19078T>A
XM_017018685.1:c.*33+57842T>A (KLRG1) XP_016874174.1:n.*33+57842T>A
NM_001347423.2:c.-18+120A>T (A2M) NP_001334352.2:n.-18+120A>T