Canonical Allele Identifier: CA2617534652

Linked Data

gnomAD v4: 12-9115999-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9115999A>T , CM000674.2:g.9115999A>T GRCh38
NC_000012.11:g.9268595A>T , CM000674.1:g.9268595A>T GRCh37
NC_000012.10:g.9159862A>T NCBI36
NG_011717.1:g.4964T>A
NG_011717.2:g.4964T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000318602.11:c.-150T>A (A2M) ENSP00000323929.7:n.-150T>A
ENST00000404455.2:c.-18+129T>A (A2M) ENSP00000385710.2:n.-18+129T>A
ENST00000467091.1:n.63T>A (A2M)
ENST00000497324.1:n.19T>A (A2M)
NM_000014.5:c.-150T>A (A2M) NP_000005.2:n.-150T>A
NM_001347423.1:c.-18+129T>A (A2M) NP_001334352.1:n.-18+129T>A
NM_001347424.1:c.-603T>A (A2M) NP_001334353.1:n.-603T>A
NM_001347425.1:c.-440T>A (A2M) NP_001334354.1:n.-440T>A
XM_017018683.1:c.*34-9375A>T (KLRG1) XP_016874172.1:n.*34-9375A>T
XM_017018684.1:c.*34-19087A>T (KLRG1) XP_016874173.1:n.*34-19087A>T
XM_017018685.1:c.*33+57833A>T (KLRG1) XP_016874174.1:n.*33+57833A>T
NM_001347423.2:c.-18+129T>A (A2M) NP_001334352.2:n.-18+129T>A