Canonical Allele Identifier: CA232699927

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs965356780
• MyVariant Identifiers: chr12:g.9268732T>C (hg19) ; chr12:g.9116136T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9116136T>C , CM000674.2:g.9116136T>C	GRCh38
NC_000012.11:g.9268732T>C , CM000674.1:g.9268732T>C	GRCh37
NC_000012.10:g.9159999T>C	NCBI36
NG_011717.1:g.4827A>G
NG_011717.2:g.4827A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.11:c.-287A>G (A2M)	ENSP00000323929.7:n.-287A>G
ENST00000404455.2:c.-26A>G (A2M)	ENSP00000385710.2:n.-26A>G
NM_000014.5:c.-287A>G (A2M)	NP_000005.2:n.-287A>G
NM_001347423.1:c.-26A>G (A2M)	NP_001334352.1:n.-26A>G
NM_001347424.1:c.-740A>G (A2M)	NP_001334353.1:n.-740A>G
NM_001347425.1:c.-577A>G (A2M)	NP_001334354.1:n.-577A>G
XM_017018683.1:c.*34-9238T>C (KLRG1)	XP_016874172.1:n.*34-9238T>C
XM_017018684.1:c.*34-18950T>C (KLRG1)	XP_016874173.1:n.*34-18950T>C
XM_017018685.1:c.*33+57970T>C (KLRG1)	XP_016874174.1:n.*33+57970T>C
NM_001347423.2:c.-26A>G (A2M)	NP_001334352.2:n.-26A>G