Canonical Allele Identifier: CA232699843

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs17201863
• gnomAD v3: 12-9116096-A-G
• gnomAD v4: 12-9116096-A-G
• MyVariant Identifiers: chr12:g.9268692A>G (hg19) ; chr12:g.9116096A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9116096A>G , CM000674.2:g.9116096A>G	GRCh38
NC_000012.11:g.9268692A>G , CM000674.1:g.9268692A>G	GRCh37
NC_000012.10:g.9159959A>G	NCBI36
NG_011717.1:g.4867T>C
NG_011717.2:g.4867T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.11:c.-247T>C (A2M)	ENSP00000323929.7:n.-247T>C
ENST00000404455.2:c.-18+32T>C (A2M)	ENSP00000385710.2:n.-18+32T>C
NM_000014.5:c.-247T>C (A2M)	NP_000005.2:n.-247T>C
NM_001347423.1:c.-18+32T>C (A2M)	NP_001334352.1:n.-18+32T>C
NM_001347424.1:c.-700T>C (A2M)	NP_001334353.1:n.-700T>C
NM_001347425.1:c.-537T>C (A2M)	NP_001334354.1:n.-537T>C
XM_017018683.1:c.*34-9278A>G (KLRG1)	XP_016874172.1:n.*34-9278A>G
XM_017018684.1:c.*34-18990A>G (KLRG1)	XP_016874173.1:n.*34-18990A>G
XM_017018685.1:c.*33+57930A>G (KLRG1)	XP_016874174.1:n.*33+57930A>G
NM_001347423.2:c.-18+32T>C (A2M)	NP_001334352.2:n.-18+32T>C