Canonical Allele Identifier: CA232700089

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs915112312
• MyVariant Identifiers: chr12:g.9268808T>C (hg19) ; chr12:g.9116212T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9116212T>C , CM000674.2:g.9116212T>C	GRCh38
NC_000012.11:g.9268808T>C , CM000674.1:g.9268808T>C	GRCh37
NC_000012.10:g.9160075T>C	NCBI36
NG_011717.1:g.4751A>G
NG_011717.2:g.4751A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404455.2:c.-102A>G (A2M)	ENSP00000385710.2:n.-102A>G
NM_000014.5:c.-363A>G (A2M)	NP_000005.2:n.-363A>G
NM_001347423.1:c.-102A>G (A2M)	NP_001334352.1:n.-102A>G
NM_001347424.1:c.-816A>G (A2M)	NP_001334353.1:n.-816A>G
NM_001347425.1:c.-653A>G (A2M)	NP_001334354.1:n.-653A>G
XM_017018683.1:c.*34-9162T>C (KLRG1)	XP_016874172.1:n.*34-9162T>C
XM_017018684.1:c.*34-18874T>C (KLRG1)	XP_016874173.1:n.*34-18874T>C
XM_017018685.1:c.*33+58046T>C (KLRG1)	XP_016874174.1:n.*33+58046T>C
NM_001347423.2:c.-102A>G (A2M)	NP_001334352.2:n.-102A>G