Canonical Allele Identifier: CA6439098

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs745394864
• ExAC: 12:9268504 C / A
• gnomAD v2: 12-9268504-C-A
• gnomAD v4: 12-9115908-C-A
• MyVariant Identifiers: chr12:g.9268504C>A (hg19) ; chr12:g.9115908C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115908C>A , CM000674.2:g.9115908C>A	GRCh38
NC_000012.11:g.9268504C>A , CM000674.1:g.9268504C>A	GRCh37
NC_000012.10:g.9159771C>A	NCBI36
NG_011717.1:g.5055G>T
NG_011717.2:g.5055G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318602.12:c.-59G>T (A2M) MANE Select	ENSP00000323929.8:n.-59G>T
ENST00000318602.11:c.-59G>T (A2M)	ENSP00000323929.7:n.-59G>T
ENST00000404455.2:c.-17-42G>T (A2M)	ENSP00000385710.2:n.-17-42G>T
ENST00000467091.1:n.154G>T (A2M)
ENST00000497324.1:n.110G>T (A2M)
NM_000014.4:c.-59G>T (A2M)	NP_000005.2:n.-59G>T
XM_006719056.2:c.-59G>T (A2M)	XP_006719119.1:n.-59G>T
NM_000014.5:c.-59G>T (A2M)	NP_000005.2:n.-59G>T
NM_001347423.1:c.-17-42G>T (A2M)	NP_001334352.1:n.-17-42G>T
NM_001347424.1:c.-512G>T (A2M)	NP_001334353.1:n.-512G>T
NM_001347425.1:c.-349G>T (A2M)	NP_001334354.1:n.-349G>T
XM_006719056.3:c.-59G>T (A2M)	XP_006719119.1:n.-59G>T
XM_017018683.1:c.*34-9466C>A (KLRG1)	XP_016874172.1:n.*34-9466C>A
XM_017018684.1:c.*34-19178C>A (KLRG1)	XP_016874173.1:n.*34-19178C>A
XM_017018685.1:c.*33+57742C>A (KLRG1)	XP_016874174.1:n.*33+57742C>A
NM_000014.6:c.-59G>T (A2M) MANE Select	NP_000005.3:n.-59G>T
NM_001347423.2:c.-17-42G>T (A2M)	NP_001334352.2:n.-17-42G>T
NM_001347424.2:c.-512G>T (A2M)	NP_001334353.2:n.-512G>T
NM_001347425.2:c.-349G>T (A2M)	NP_001334354.2:n.-349G>T