Canonical Allele Identifier: CA2617534669

Linked Data

gnomAD v4: 12-9116012-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116012T>C , CM000674.2:g.9116012T>C GRCh38
NC_000012.11:g.9268608T>C , CM000674.1:g.9268608T>C GRCh37
NC_000012.10:g.9159875T>C NCBI36
NG_011717.1:g.4951A>G
NG_011717.2:g.4951A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000318602.11:c.-163A>G (A2M) ENSP00000323929.7:n.-163A>G
ENST00000404455.2:c.-18+116A>G (A2M) ENSP00000385710.2:n.-18+116A>G
ENST00000467091.1:n.50A>G (A2M)
ENST00000497324.1:n.6A>G (A2M)
NM_000014.5:c.-163A>G (A2M) NP_000005.2:n.-163A>G
NM_001347423.1:c.-18+116A>G (A2M) NP_001334352.1:n.-18+116A>G
NM_001347424.1:c.-616A>G (A2M) NP_001334353.1:n.-616A>G
NM_001347425.1:c.-453A>G (A2M) NP_001334354.1:n.-453A>G
XM_017018683.1:c.*34-9362T>C (KLRG1) XP_016874172.1:n.*34-9362T>C
XM_017018684.1:c.*34-19074T>C (KLRG1) XP_016874173.1:n.*34-19074T>C
XM_017018685.1:c.*33+57846T>C (KLRG1) XP_016874174.1:n.*33+57846T>C
NM_001347423.2:c.-18+116A>G (A2M) NP_001334352.2:n.-18+116A>G