Canonical Allele Identifier: CA944576248

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs1939101405
• gnomAD v4: 12-9116123-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9116123C>T , CM000674.2:g.9116123C>T	GRCh38
NC_000012.11:g.9268719C>T , CM000674.1:g.9268719C>T	GRCh37
NC_000012.10:g.9159986C>T	NCBI36
NG_011717.1:g.4840G>A
NG_011717.2:g.4840G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.11:c.-274G>A (A2M)	ENSP00000323929.7:n.-274G>A
ENST00000404455.2:c.-18+5G>A (A2M)	ENSP00000385710.2:n.-18+5G>A
NM_000014.5:c.-274G>A (A2M)	NP_000005.2:n.-274G>A
NM_001347423.1:c.-18+5G>A (A2M)	NP_001334352.1:n.-18+5G>A
NM_001347424.1:c.-727G>A (A2M)	NP_001334353.1:n.-727G>A
NM_001347425.1:c.-564G>A (A2M)	NP_001334354.1:n.-564G>A
XM_017018683.1:c.*34-9251C>T (KLRG1)	XP_016874172.1:n.*34-9251C>T
XM_017018684.1:c.*34-18963C>T (KLRG1)	XP_016874173.1:n.*34-18963C>T
XM_017018685.1:c.*33+57957C>T (KLRG1)	XP_016874174.1:n.*33+57957C>T
NM_001347423.2:c.-18+5G>A (A2M)	NP_001334352.2:n.-18+5G>A