Canonical Allele Identifier: CA2015347067

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116046T= , CM000674.2:g.9116046T= GRCh38
NC_000012.11:g.9268642T= , CM000674.1:g.9268642T= GRCh37
NC_000012.10:g.9159909T= NCBI36
NG_011717.1:g.4917A=
NG_011717.2:g.4917A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-197A= (A2M) ENSP00000323929.7:n.-197A=
ENST00000404455.2:c.-18+82A= (A2M) ENSP00000385710.2:n.-18+82A=
ENST00000467091.1:n.16A= (A2M)
NM_000014.5:c.-197A= (A2M) NP_000005.2:n.-197A=
NM_001347423.1:c.-18+82A= (A2M) NP_001334352.1:n.-18+82A=
NM_001347424.1:c.-650A= (A2M) NP_001334353.1:n.-650A=
NM_001347425.1:c.-487A= (A2M) NP_001334354.1:n.-487A=
XM_017018683.1:c.*34-9328T= (KLRG1) XP_016874172.1:n.*34-9328T=
XM_017018684.1:c.*34-19040T= (KLRG1) XP_016874173.1:n.*34-19040T=
XM_017018685.1:c.*33+57880T= (KLRG1) XP_016874174.1:n.*33+57880T=
NM_001347423.2:c.-18+82A= (A2M) NP_001334352.2:n.-18+82A=