Canonical Allele Identifier: CA2015347129

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116182C= , CM000674.2:g.9116182C= GRCh38
NC_000012.11:g.9268778C= , CM000674.1:g.9268778C= GRCh37
NC_000012.10:g.9160045C= NCBI36
NG_011717.1:g.4781G=
NG_011717.2:g.4781G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-72G= (A2M) ENSP00000385710.2:n.-72G=
NM_000014.5:c.-333G= (A2M) NP_000005.2:n.-333G=
NM_001347423.1:c.-72G= (A2M) NP_001334352.1:n.-72G=
NM_001347424.1:c.-786G= (A2M) NP_001334353.1:n.-786G=
NM_001347425.1:c.-623G= (A2M) NP_001334354.1:n.-623G=
XM_017018683.1:c.*34-9192C= (KLRG1) XP_016874172.1:n.*34-9192C=
XM_017018684.1:c.*34-18904C= (KLRG1) XP_016874173.1:n.*34-18904C=
XM_017018685.1:c.*33+58016C= (KLRG1) XP_016874174.1:n.*33+58016C=
NM_001347423.2:c.-72G= (A2M) NP_001334352.2:n.-72G=