Canonical Allele Identifier: CA232699779

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs915718714
• gnomAD v2: 12-9268536-G-A
• gnomAD v3: 12-9115940-G-A
• gnomAD v4: 12-9115940-G-A
• MyVariant Identifiers: chr12:g.9268536G>A (hg19) ; chr12:g.9115940G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115940G>A , CM000674.2:g.9115940G>A	GRCh38
NC_000012.11:g.9268536G>A , CM000674.1:g.9268536G>A	GRCh37
NC_000012.10:g.9159803G>A	NCBI36
NG_011717.1:g.5023C>T
NG_011717.2:g.5023C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.11:c.-91C>T (A2M)	ENSP00000323929.7:n.-91C>T
ENST00000404455.2:c.-17-74C>T (A2M)	ENSP00000385710.2:n.-17-74C>T
ENST00000467091.1:n.122C>T (A2M)
ENST00000497324.1:n.78C>T (A2M)
NM_000014.4:c.-91C>T (A2M)	NP_000005.2:n.-91C>T
XM_006719056.2:c.-91C>T (A2M)	XP_006719119.1:n.-91C>T
NM_000014.5:c.-91C>T (A2M)	NP_000005.2:n.-91C>T
NM_001347423.1:c.-17-74C>T (A2M)	NP_001334352.1:n.-17-74C>T
NM_001347424.1:c.-544C>T (A2M)	NP_001334353.1:n.-544C>T
NM_001347425.1:c.-381C>T (A2M)	NP_001334354.1:n.-381C>T
XM_006719056.3:c.-91C>T (A2M)	XP_006719119.1:n.-91C>T
XM_017018683.1:c.*34-9434G>A (KLRG1)	XP_016874172.1:n.*34-9434G>A
XM_017018684.1:c.*34-19146G>A (KLRG1)	XP_016874173.1:n.*34-19146G>A
XM_017018685.1:c.*33+57774G>A (KLRG1)	XP_016874174.1:n.*33+57774G>A
NM_001347423.2:c.-17-74C>T (A2M)	NP_001334352.2:n.-17-74C>T