Canonical Allele Identifier: CA2794496568

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116195A>G , CM000674.2:g.9116195A>G GRCh38
NC_000012.11:g.9268791A>G , CM000674.1:g.9268791A>G GRCh37
NC_000012.10:g.9160058A>G NCBI36
NG_011717.1:g.4768T>C
NG_011717.2:g.4768T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-85T>C (A2M) ENSP00000385710.2:n.-85T>C
NM_000014.5:c.-346T>C (A2M) NP_000005.2:n.-346T>C
NM_001347423.1:c.-85T>C (A2M) NP_001334352.1:n.-85T>C
NM_001347424.1:c.-799T>C (A2M) NP_001334353.1:n.-799T>C
NM_001347425.1:c.-636T>C (A2M) NP_001334354.1:n.-636T>C
XM_017018683.1:c.*34-9179A>G (KLRG1) XP_016874172.1:n.*34-9179A>G
XM_017018684.1:c.*34-18891A>G (KLRG1) XP_016874173.1:n.*34-18891A>G
XM_017018685.1:c.*33+58029A>G (KLRG1) XP_016874174.1:n.*33+58029A>G
NM_001347423.2:c.-85T>C (A2M) NP_001334352.2:n.-85T>C