Canonical Allele Identifier: CA2617534928

Linked Data

gnomAD v4: 12-9116218-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116218C>A , CM000674.2:g.9116218C>A GRCh38
NC_000012.11:g.9268814C>A , CM000674.1:g.9268814C>A GRCh37
NC_000012.10:g.9160081C>A NCBI36
NG_011717.1:g.4745G>T
NG_011717.2:g.4745G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-108G>T (A2M) ENSP00000385710.2:n.-108G>T
NM_000014.5:c.-369G>T (A2M) NP_000005.2:n.-369G>T
NM_001347423.1:c.-108G>T (A2M) NP_001334352.1:n.-108G>T
NM_001347424.1:c.-822G>T (A2M) NP_001334353.1:n.-822G>T
NM_001347425.1:c.-659G>T (A2M) NP_001334354.1:n.-659G>T
XM_017018683.1:c.*34-9156C>A (KLRG1) XP_016874172.1:n.*34-9156C>A
XM_017018684.1:c.*34-18868C>A (KLRG1) XP_016874173.1:n.*34-18868C>A
XM_017018685.1:c.*33+58052C>A (KLRG1) XP_016874174.1:n.*33+58052C>A
NM_001347423.2:c.-108G>T (A2M) NP_001334352.2:n.-108G>T