Canonical Allele Identifier: CA2015347122

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116170C= , CM000674.2:g.9116170C= GRCh38
NC_000012.11:g.9268766C= , CM000674.1:g.9268766C= GRCh37
NC_000012.10:g.9160033C= NCBI36
NG_011717.1:g.4793G=
NG_011717.2:g.4793G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-60G= (A2M) ENSP00000385710.2:n.-60G=
NM_000014.5:c.-321G= (A2M) NP_000005.2:n.-321G=
NM_001347423.1:c.-60G= (A2M) NP_001334352.1:n.-60G=
NM_001347424.1:c.-774G= (A2M) NP_001334353.1:n.-774G=
NM_001347425.1:c.-611G= (A2M) NP_001334354.1:n.-611G=
XM_017018683.1:c.*34-9204C= (KLRG1) XP_016874172.1:n.*34-9204C=
XM_017018684.1:c.*34-18916C= (KLRG1) XP_016874173.1:n.*34-18916C=
XM_017018685.1:c.*33+58004C= (KLRG1) XP_016874174.1:n.*33+58004C=
NM_001347423.2:c.-60G= (A2M) NP_001334352.2:n.-60G=