Canonical Allele Identifier: CA2015347128

Linked Data

dbSNP Id: rs1939106285

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116180C>T , CM000674.2:g.9116180C>T GRCh38
NC_000012.11:g.9268776C>T , CM000674.1:g.9268776C>T GRCh37
NC_000012.10:g.9160043C>T NCBI36
NG_011717.1:g.4783G>A
NG_011717.2:g.4783G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-70G>A (A2M) ENSP00000385710.2:n.-70G>A
NM_000014.5:c.-331G>A (A2M) NP_000005.2:n.-331G>A
NM_001347423.1:c.-70G>A (A2M) NP_001334352.1:n.-70G>A
NM_001347424.1:c.-784G>A (A2M) NP_001334353.1:n.-784G>A
NM_001347425.1:c.-621G>A (A2M) NP_001334354.1:n.-621G>A
XM_017018683.1:c.*34-9194C>T (KLRG1) XP_016874172.1:n.*34-9194C>T
XM_017018684.1:c.*34-18906C>T (KLRG1) XP_016874173.1:n.*34-18906C>T
XM_017018685.1:c.*33+58014C>T (KLRG1) XP_016874174.1:n.*33+58014C>T
NM_001347423.2:c.-70G>A (A2M) NP_001334352.2:n.-70G>A