Canonical Allele Identifier: CA2015347021

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs1939089926
• gnomAD v4: 12-9115951-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115951T>C , CM000674.2:g.9115951T>C	GRCh38
NC_000012.11:g.9268547T>C , CM000674.1:g.9268547T>C	GRCh37
NC_000012.10:g.9159814T>C	NCBI36
NG_011717.1:g.5012A>G
NG_011717.2:g.5012A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.11:c.-102A>G (A2M)	ENSP00000323929.7:n.-102A>G
ENST00000404455.2:c.-17-85A>G (A2M)	ENSP00000385710.2:n.-17-85A>G
ENST00000467091.1:n.111A>G (A2M)
ENST00000497324.1:n.67A>G (A2M)
NM_000014.4:c.-102A>G (A2M)	NP_000005.2:n.-102A>G
NM_000014.5:c.-102A>G (A2M)	NP_000005.2:n.-102A>G
NM_001347423.1:c.-17-85A>G (A2M)	NP_001334352.1:n.-17-85A>G
NM_001347424.1:c.-555A>G (A2M)	NP_001334353.1:n.-555A>G
NM_001347425.1:c.-392A>G (A2M)	NP_001334354.1:n.-392A>G
XM_017018683.1:c.*34-9423T>C (KLRG1)	XP_016874172.1:n.*34-9423T>C
XM_017018684.1:c.*34-19135T>C (KLRG1)	XP_016874173.1:n.*34-19135T>C
XM_017018685.1:c.*33+57785T>C (KLRG1)	XP_016874174.1:n.*33+57785T>C
NM_001347423.2:c.-17-85A>G (A2M)	NP_001334352.2:n.-17-85A>G