Canonical Allele Identifier: CA2015347130

Linked Data

dbSNP Id: rs921377538
gnomAD v4: 12-9116182-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116182C>A , CM000674.2:g.9116182C>A GRCh38
NC_000012.11:g.9268778C>A , CM000674.1:g.9268778C>A GRCh37
NC_000012.10:g.9160045C>A NCBI36
NG_011717.1:g.4781G>T
NG_011717.2:g.4781G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-72G>T (A2M) ENSP00000385710.2:n.-72G>T
NM_000014.5:c.-333G>T (A2M) NP_000005.2:n.-333G>T
NM_001347423.1:c.-72G>T (A2M) NP_001334352.1:n.-72G>T
NM_001347424.1:c.-786G>T (A2M) NP_001334353.1:n.-786G>T
NM_001347425.1:c.-623G>T (A2M) NP_001334354.1:n.-623G>T
XM_017018683.1:c.*34-9192C>A (KLRG1) XP_016874172.1:n.*34-9192C>A
XM_017018684.1:c.*34-18904C>A (KLRG1) XP_016874173.1:n.*34-18904C>A
XM_017018685.1:c.*33+58016C>A (KLRG1) XP_016874174.1:n.*33+58016C>A
NM_001347423.2:c.-72G>T (A2M) NP_001334352.2:n.-72G>T