Canonical Allele Identifier: CA2015347149

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116223C= , CM000674.2:g.9116223C= GRCh38
NC_000012.11:g.9268819C= , CM000674.1:g.9268819C= GRCh37
NC_000012.10:g.9160086C= NCBI36
NG_011717.1:g.4740G=
NG_011717.2:g.4740G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-113G= (A2M) ENSP00000385710.2:n.-113G=
NM_000014.5:c.-374G= (A2M) NP_000005.2:n.-374G=
NM_001347423.1:c.-113G= (A2M) NP_001334352.1:n.-113G=
NM_001347424.1:c.-827G= (A2M) NP_001334353.1:n.-827G=
NM_001347425.1:c.-664G= (A2M) NP_001334354.1:n.-664G=
XM_017018683.1:c.*34-9151C= (KLRG1) XP_016874172.1:n.*34-9151C=
XM_017018684.1:c.*34-18863C= (KLRG1) XP_016874173.1:n.*34-18863C=
XM_017018685.1:c.*33+58057C= (KLRG1) XP_016874174.1:n.*33+58057C=
NM_001347423.2:c.-113G= (A2M) NP_001334352.2:n.-113G=