Canonical Allele Identifier: CA2015347151

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116227T= , CM000674.2:g.9116227T= GRCh38
NC_000012.11:g.9268823T= , CM000674.1:g.9268823T= GRCh37
NC_000012.10:g.9160090T= NCBI36
NG_011717.1:g.4736A=
NG_011717.2:g.4736A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-117A= (A2M) ENSP00000385710.2:n.-117A=
NM_000014.5:c.-378A= (A2M) NP_000005.2:n.-378A=
NM_001347423.1:c.-117A= (A2M) NP_001334352.1:n.-117A=
NM_001347424.1:c.-831A= (A2M) NP_001334353.1:n.-831A=
NM_001347425.1:c.-668A= (A2M) NP_001334354.1:n.-668A=
XM_017018683.1:c.*34-9147T= (KLRG1) XP_016874172.1:n.*34-9147T=
XM_017018684.1:c.*34-18859T= (KLRG1) XP_016874173.1:n.*34-18859T=
XM_017018685.1:c.*33+58061T= (KLRG1) XP_016874174.1:n.*33+58061T=
NM_001347423.2:c.-117A= (A2M) NP_001334352.2:n.-117A=