Canonical Allele Identifier: CA232699832

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs576073841
• gnomAD v4: 12-9116037-A-G
• MyVariant Identifiers: chr12:g.9268633A>G (hg19) ; chr12:g.9116037A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9116037A>G , CM000674.2:g.9116037A>G	GRCh38
NC_000012.11:g.9268633A>G , CM000674.1:g.9268633A>G	GRCh37
NC_000012.10:g.9159900A>G	NCBI36
NG_011717.1:g.4926T>C
NG_011717.2:g.4926T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.11:c.-188T>C (A2M)	ENSP00000323929.7:n.-188T>C
ENST00000404455.2:c.-18+91T>C (A2M)	ENSP00000385710.2:n.-18+91T>C
ENST00000467091.1:n.25T>C (A2M)
NM_000014.5:c.-188T>C (A2M)	NP_000005.2:n.-188T>C
NM_001347423.1:c.-18+91T>C (A2M)	NP_001334352.1:n.-18+91T>C
NM_001347424.1:c.-641T>C (A2M)	NP_001334353.1:n.-641T>C
NM_001347425.1:c.-478T>C (A2M)	NP_001334354.1:n.-478T>C
XM_017018683.1:c.*34-9337A>G (KLRG1)	XP_016874172.1:n.*34-9337A>G
XM_017018684.1:c.*34-19049A>G (KLRG1)	XP_016874173.1:n.*34-19049A>G
XM_017018685.1:c.*33+57871A>G (KLRG1)	XP_016874174.1:n.*33+57871A>G
NM_001347423.2:c.-18+91T>C (A2M)	NP_001334352.2:n.-18+91T>C