Canonical Allele Identifier: CA6439101

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs186546405
• ExAC: 12:9268508 C / T
• gnomAD v2: 12-9268508-C-T
• gnomAD v4: 12-9115912-C-T
• MyVariant Identifiers: chr12:g.9268508C>T (hg19) ; chr12:g.9115912C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115912C>T , CM000674.2:g.9115912C>T	GRCh38
NC_000012.11:g.9268508C>T , CM000674.1:g.9268508C>T	GRCh37
NC_000012.10:g.9159775C>T	NCBI36
NG_011717.1:g.5051G>A
NG_011717.2:g.5051G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318602.12:c.-63G>A (A2M) MANE Select	ENSP00000323929.8:n.-63G>A
ENST00000318602.11:c.-63G>A (A2M)	ENSP00000323929.7:n.-63G>A
ENST00000404455.2:c.-17-46G>A (A2M)	ENSP00000385710.2:n.-17-46G>A
ENST00000467091.1:n.150G>A (A2M)
ENST00000497324.1:n.106G>A (A2M)
NM_000014.4:c.-63G>A (A2M)	NP_000005.2:n.-63G>A
XM_006719056.2:c.-63G>A (A2M)	XP_006719119.1:n.-63G>A
NM_000014.5:c.-63G>A (A2M)	NP_000005.2:n.-63G>A
NM_001347423.1:c.-17-46G>A (A2M)	NP_001334352.1:n.-17-46G>A
NM_001347424.1:c.-516G>A (A2M)	NP_001334353.1:n.-516G>A
NM_001347425.1:c.-353G>A (A2M)	NP_001334354.1:n.-353G>A
XM_006719056.3:c.-63G>A (A2M)	XP_006719119.1:n.-63G>A
XM_017018683.1:c.*34-9462C>T (KLRG1)	XP_016874172.1:n.*34-9462C>T
XM_017018684.1:c.*34-19174C>T (KLRG1)	XP_016874173.1:n.*34-19174C>T
XM_017018685.1:c.*33+57746C>T (KLRG1)	XP_016874174.1:n.*33+57746C>T
NM_000014.6:c.-63G>A (A2M) MANE Select	NP_000005.3:n.-63G>A
NM_001347423.2:c.-17-46G>A (A2M)	NP_001334352.2:n.-17-46G>A
NM_001347424.2:c.-516G>A (A2M)	NP_001334353.2:n.-516G>A
NM_001347425.2:c.-353G>A (A2M)	NP_001334354.2:n.-353G>A