Canonical Allele Identifier: CA944576209

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs1939095292
• gnomAD v3: 12-9116022-C-T
• gnomAD v4: 12-9116022-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9116022C>T , CM000674.2:g.9116022C>T	GRCh38
NC_000012.11:g.9268618C>T , CM000674.1:g.9268618C>T	GRCh37
NC_000012.10:g.9159885C>T	NCBI36
NG_011717.1:g.4941G>A
NG_011717.2:g.4941G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.11:c.-173G>A (A2M)	ENSP00000323929.7:n.-173G>A
ENST00000404455.2:c.-18+106G>A (A2M)	ENSP00000385710.2:n.-18+106G>A
ENST00000467091.1:n.40G>A (A2M)
NM_000014.5:c.-173G>A (A2M)	NP_000005.2:n.-173G>A
NM_001347423.1:c.-18+106G>A (A2M)	NP_001334352.1:n.-18+106G>A
NM_001347424.1:c.-626G>A (A2M)	NP_001334353.1:n.-626G>A
NM_001347425.1:c.-463G>A (A2M)	NP_001334354.1:n.-463G>A
XM_017018683.1:c.*34-9352C>T (KLRG1)	XP_016874172.1:n.*34-9352C>T
XM_017018684.1:c.*34-19064C>T (KLRG1)	XP_016874173.1:n.*34-19064C>T
XM_017018685.1:c.*33+57856C>T (KLRG1)	XP_016874174.1:n.*33+57856C>T
NM_001347423.2:c.-18+106G>A (A2M)	NP_001334352.2:n.-18+106G>A