Canonical Allele Identifier: CA2015347123

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116172C= , CM000674.2:g.9116172C= GRCh38
NC_000012.11:g.9268768C= , CM000674.1:g.9268768C= GRCh37
NC_000012.10:g.9160035C= NCBI36
NG_011717.1:g.4791G=
NG_011717.2:g.4791G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-62G= (A2M) ENSP00000385710.2:n.-62G=
NM_000014.5:c.-323G= (A2M) NP_000005.2:n.-323G=
NM_001347423.1:c.-62G= (A2M) NP_001334352.1:n.-62G=
NM_001347424.1:c.-776G= (A2M) NP_001334353.1:n.-776G=
NM_001347425.1:c.-613G= (A2M) NP_001334354.1:n.-613G=
XM_017018683.1:c.*34-9202C= (KLRG1) XP_016874172.1:n.*34-9202C=
XM_017018684.1:c.*34-18914C= (KLRG1) XP_016874173.1:n.*34-18914C=
XM_017018685.1:c.*33+58006C= (KLRG1) XP_016874174.1:n.*33+58006C=
NM_001347423.2:c.-62G= (A2M) NP_001334352.2:n.-62G=