Canonical Allele Identifier: CA232699736

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs111797190
• MyVariant Identifiers: chr12:g.9268516A>C (hg19) ; chr12:g.9115920A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115920A>C , CM000674.2:g.9115920A>C	GRCh38
NC_000012.11:g.9268516A>C , CM000674.1:g.9268516A>C	GRCh37
NC_000012.10:g.9159783A>C	NCBI36
NG_011717.1:g.5043T>G
NG_011717.2:g.5043T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.11:c.-71T>G (A2M)	ENSP00000323929.7:n.-71T>G
ENST00000404455.2:c.-17-54T>G (A2M)	ENSP00000385710.2:n.-17-54T>G
ENST00000467091.1:n.142T>G (A2M)
ENST00000497324.1:n.98T>G (A2M)
NM_000014.4:c.-71T>G (A2M)	NP_000005.2:n.-71T>G
XM_006719056.2:c.-71T>G (A2M)	XP_006719119.1:n.-71T>G
NM_000014.5:c.-71T>G (A2M)	NP_000005.2:n.-71T>G
NM_001347423.1:c.-17-54T>G (A2M)	NP_001334352.1:n.-17-54T>G
NM_001347424.1:c.-524T>G (A2M)	NP_001334353.1:n.-524T>G
NM_001347425.1:c.-361T>G (A2M)	NP_001334354.1:n.-361T>G
XM_006719056.3:c.-71T>G (A2M)	XP_006719119.1:n.-71T>G
XM_017018683.1:c.*34-9454A>C (KLRG1)	XP_016874172.1:n.*34-9454A>C
XM_017018684.1:c.*34-19166A>C (KLRG1)	XP_016874173.1:n.*34-19166A>C
XM_017018685.1:c.*33+57754A>C (KLRG1)	XP_016874174.1:n.*33+57754A>C
NM_001347423.2:c.-17-54T>G (A2M)	NP_001334352.2:n.-17-54T>G