Canonical Allele Identifier: CA6439097

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs780553476
• ExAC: 12:9268503 T / C
• gnomAD v2: 12-9268503-T-C
• gnomAD v3: 12-9115907-T-C
• gnomAD v4: 12-9115907-T-C
• MyVariant Identifiers: chr12:g.9268503T>C (hg19) ; chr12:g.9115907T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115907T>C , CM000674.2:g.9115907T>C	GRCh38
NC_000012.11:g.9268503T>C , CM000674.1:g.9268503T>C	GRCh37
NC_000012.10:g.9159770T>C	NCBI36
NG_011717.1:g.5056A>G
NG_011717.2:g.5056A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.-58A>G (A2M) MANE Select	ENSP00000323929.8:n.-58A>G
ENST00000318602.11:c.-58A>G (A2M)	ENSP00000323929.7:n.-58A>G
ENST00000404455.2:c.-17-41A>G (A2M)	ENSP00000385710.2:n.-17-41A>G
ENST00000467091.1:n.155A>G (A2M)
ENST00000497324.1:n.111A>G (A2M)
NM_000014.4:c.-58A>G (A2M)	NP_000005.2:n.-58A>G
XM_006719056.2:c.-58A>G (A2M)	XP_006719119.1:n.-58A>G
NM_000014.5:c.-58A>G (A2M)	NP_000005.2:n.-58A>G
NM_001347423.1:c.-17-41A>G (A2M)	NP_001334352.1:n.-17-41A>G
NM_001347424.1:c.-511A>G (A2M)	NP_001334353.1:n.-511A>G
NM_001347425.1:c.-348A>G (A2M)	NP_001334354.1:n.-348A>G
XM_006719056.3:c.-58A>G (A2M)	XP_006719119.1:n.-58A>G
XM_017018683.1:c.*34-9467T>C (KLRG1)	XP_016874172.1:n.*34-9467T>C
XM_017018684.1:c.*34-19179T>C (KLRG1)	XP_016874173.1:n.*34-19179T>C
XM_017018685.1:c.*33+57741T>C (KLRG1)	XP_016874174.1:n.*33+57741T>C
NM_000014.6:c.-58A>G (A2M) MANE Select	NP_000005.3:n.-58A>G
NM_001347423.2:c.-17-41A>G (A2M)	NP_001334352.2:n.-17-41A>G
NM_001347424.2:c.-511A>G (A2M)	NP_001334353.2:n.-511A>G
NM_001347425.2:c.-348A>G (A2M)	NP_001334354.2:n.-348A>G