Canonical Allele Identifier: CA944576245

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs1939100168
• gnomAD v3: 12-9116110-A-T
• gnomAD v4: 12-9116110-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9116110A>T , CM000674.2:g.9116110A>T	GRCh38
NC_000012.11:g.9268706A>T , CM000674.1:g.9268706A>T	GRCh37
NC_000012.10:g.9159973A>T	NCBI36
NG_011717.1:g.4853T>A
NG_011717.2:g.4853T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.11:c.-261T>A (A2M)	ENSP00000323929.7:n.-261T>A
ENST00000404455.2:c.-18+18T>A (A2M)	ENSP00000385710.2:n.-18+18T>A
NM_000014.5:c.-261T>A (A2M)	NP_000005.2:n.-261T>A
NM_001347423.1:c.-18+18T>A (A2M)	NP_001334352.1:n.-18+18T>A
NM_001347424.1:c.-714T>A (A2M)	NP_001334353.1:n.-714T>A
NM_001347425.1:c.-551T>A (A2M)	NP_001334354.1:n.-551T>A
XM_017018683.1:c.*34-9264A>T (KLRG1)	XP_016874172.1:n.*34-9264A>T
XM_017018684.1:c.*34-18976A>T (KLRG1)	XP_016874173.1:n.*34-18976A>T
XM_017018685.1:c.*33+57944A>T (KLRG1)	XP_016874174.1:n.*33+57944A>T
NM_001347423.2:c.-18+18T>A (A2M)	NP_001334352.2:n.-18+18T>A