Canonical Allele Identifier: CA2015347068

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116058T= , CM000674.2:g.9116058T= GRCh38
NC_000012.11:g.9268654T= , CM000674.1:g.9268654T= GRCh37
NC_000012.10:g.9159921T= NCBI36
NG_011717.1:g.4905A=
NG_011717.2:g.4905A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-209A= (A2M) ENSP00000323929.7:n.-209A=
ENST00000404455.2:c.-18+70A= (A2M) ENSP00000385710.2:n.-18+70A=
ENST00000467091.1:n.4A= (A2M)
NM_000014.5:c.-209A= (A2M) NP_000005.2:n.-209A=
NM_001347423.1:c.-18+70A= (A2M) NP_001334352.1:n.-18+70A=
NM_001347424.1:c.-662A= (A2M) NP_001334353.1:n.-662A=
NM_001347425.1:c.-499A= (A2M) NP_001334354.1:n.-499A=
XM_017018683.1:c.*34-9316T= (KLRG1) XP_016874172.1:n.*34-9316T=
XM_017018684.1:c.*34-19028T= (KLRG1) XP_016874173.1:n.*34-19028T=
XM_017018685.1:c.*33+57892T= (KLRG1) XP_016874174.1:n.*33+57892T=
NM_001347423.2:c.-18+70A= (A2M) NP_001334352.2:n.-18+70A=