Canonical Allele Identifier: CA2015347150

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116226G= , CM000674.2:g.9116226G= GRCh38
NC_000012.11:g.9268822G= , CM000674.1:g.9268822G= GRCh37
NC_000012.10:g.9160089G= NCBI36
NG_011717.1:g.4737C=
NG_011717.2:g.4737C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-116C= (A2M) ENSP00000385710.2:n.-116C=
NM_000014.5:c.-377C= (A2M) NP_000005.2:n.-377C=
NM_001347423.1:c.-116C= (A2M) NP_001334352.1:n.-116C=
NM_001347424.1:c.-830C= (A2M) NP_001334353.1:n.-830C=
NM_001347425.1:c.-667C= (A2M) NP_001334354.1:n.-667C=
XM_017018683.1:c.*34-9148G= (KLRG1) XP_016874172.1:n.*34-9148G=
XM_017018684.1:c.*34-18860G= (KLRG1) XP_016874173.1:n.*34-18860G=
XM_017018685.1:c.*33+58060G= (KLRG1) XP_016874174.1:n.*33+58060G=
NM_001347423.2:c.-116C= (A2M) NP_001334352.2:n.-116C=