Canonical Allele Identifier: CA232699827

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs746570953
• gnomAD v4: 12-9116013-G-A
• MyVariant Identifiers: chr12:g.9268609G>A (hg19) ; chr12:g.9116013G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9116013G>A , CM000674.2:g.9116013G>A	GRCh38
NC_000012.11:g.9268609G>A , CM000674.1:g.9268609G>A	GRCh37
NC_000012.10:g.9159876G>A	NCBI36
NG_011717.1:g.4950C>T
NG_011717.2:g.4950C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.11:c.-164C>T (A2M)	ENSP00000323929.7:n.-164C>T
ENST00000404455.2:c.-18+115C>T (A2M)	ENSP00000385710.2:n.-18+115C>T
ENST00000467091.1:n.49C>T (A2M)
ENST00000497324.1:n.5C>T (A2M)
NM_000014.5:c.-164C>T (A2M)	NP_000005.2:n.-164C>T
NM_001347423.1:c.-18+115C>T (A2M)	NP_001334352.1:n.-18+115C>T
NM_001347424.1:c.-617C>T (A2M)	NP_001334353.1:n.-617C>T
NM_001347425.1:c.-454C>T (A2M)	NP_001334354.1:n.-454C>T
XM_017018683.1:c.*34-9361G>A (KLRG1)	XP_016874172.1:n.*34-9361G>A
XM_017018684.1:c.*34-19073G>A (KLRG1)	XP_016874173.1:n.*34-19073G>A
XM_017018685.1:c.*33+57847G>A (KLRG1)	XP_016874174.1:n.*33+57847G>A
NM_001347423.2:c.-18+115C>T (A2M)	NP_001334352.2:n.-18+115C>T