Canonical Allele Identifier: CA232699979

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs977033647
• gnomAD v2: 12-9268775-C-T
• gnomAD v3: 12-9116179-C-T
• gnomAD v4: 12-9116179-C-T
• MyVariant Identifiers: chr12:g.9268775C>T (hg19) ; chr12:g.9116179C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9116179C>T , CM000674.2:g.9116179C>T	GRCh38
NC_000012.11:g.9268775C>T , CM000674.1:g.9268775C>T	GRCh37
NC_000012.10:g.9160042C>T	NCBI36
NG_011717.1:g.4784G>A
NG_011717.2:g.4784G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404455.2:c.-69G>A (A2M)	ENSP00000385710.2:n.-69G>A
NM_000014.5:c.-330G>A (A2M)	NP_000005.2:n.-330G>A
NM_001347423.1:c.-69G>A (A2M)	NP_001334352.1:n.-69G>A
NM_001347424.1:c.-783G>A (A2M)	NP_001334353.1:n.-783G>A
NM_001347425.1:c.-620G>A (A2M)	NP_001334354.1:n.-620G>A
XM_017018683.1:c.*34-9195C>T (KLRG1)	XP_016874172.1:n.*34-9195C>T
XM_017018684.1:c.*34-18907C>T (KLRG1)	XP_016874173.1:n.*34-18907C>T
XM_017018685.1:c.*33+58013C>T (KLRG1)	XP_016874174.1:n.*33+58013C>T
NM_001347423.2:c.-69G>A (A2M)	NP_001334352.2:n.-69G>A