Canonical Allele Identifier: CA2794496565

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116143G>C , CM000674.2:g.9116143G>C GRCh38
NC_000012.11:g.9268739G>C , CM000674.1:g.9268739G>C GRCh37
NC_000012.10:g.9160006G>C NCBI36
NG_011717.1:g.4820C>G
NG_011717.2:g.4820C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-294C>G (A2M) ENSP00000323929.7:n.-294C>G
ENST00000404455.2:c.-33C>G (A2M) ENSP00000385710.2:n.-33C>G
NM_000014.5:c.-294C>G (A2M) NP_000005.2:n.-294C>G
NM_001347423.1:c.-33C>G (A2M) NP_001334352.1:n.-33C>G
NM_001347424.1:c.-747C>G (A2M) NP_001334353.1:n.-747C>G
NM_001347425.1:c.-584C>G (A2M) NP_001334354.1:n.-584C>G
XM_017018683.1:c.*34-9231G>C (KLRG1) XP_016874172.1:n.*34-9231G>C
XM_017018684.1:c.*34-18943G>C (KLRG1) XP_016874173.1:n.*34-18943G>C
XM_017018685.1:c.*33+57977G>C (KLRG1) XP_016874174.1:n.*33+57977G>C
NM_001347423.2:c.-33C>G (A2M) NP_001334352.2:n.-33C>G