Canonical Allele Identifier: CA2015347062

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116037A= , CM000674.2:g.9116037A= GRCh38
NC_000012.11:g.9268633A= , CM000674.1:g.9268633A= GRCh37
NC_000012.10:g.9159900A= NCBI36
NG_011717.1:g.4926T=
NG_011717.2:g.4926T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-188T= (A2M) ENSP00000323929.7:n.-188T=
ENST00000404455.2:c.-18+91T= (A2M) ENSP00000385710.2:n.-18+91T=
ENST00000467091.1:n.25T= (A2M)
NM_000014.5:c.-188T= (A2M) NP_000005.2:n.-188T=
NM_001347423.1:c.-18+91T= (A2M) NP_001334352.1:n.-18+91T=
NM_001347424.1:c.-641T= (A2M) NP_001334353.1:n.-641T=
NM_001347425.1:c.-478T= (A2M) NP_001334354.1:n.-478T=
XM_017018683.1:c.*34-9337A= (KLRG1) XP_016874172.1:n.*34-9337A=
XM_017018684.1:c.*34-19049A= (KLRG1) XP_016874173.1:n.*34-19049A=
XM_017018685.1:c.*33+57871A= (KLRG1) XP_016874174.1:n.*33+57871A=
NM_001347423.2:c.-18+91T= (A2M) NP_001334352.2:n.-18+91T=