Canonical Allele Identifier: CA2617534884

Linked Data

gnomAD v4: 12-9116186-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116186A>T , CM000674.2:g.9116186A>T GRCh38
NC_000012.11:g.9268782A>T , CM000674.1:g.9268782A>T GRCh37
NC_000012.10:g.9160049A>T NCBI36
NG_011717.1:g.4777T>A
NG_011717.2:g.4777T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000404455.2:c.-76T>A (A2M) ENSP00000385710.2:n.-76T>A
NM_000014.5:c.-337T>A (A2M) NP_000005.2:n.-337T>A
NM_001347423.1:c.-76T>A (A2M) NP_001334352.1:n.-76T>A
NM_001347424.1:c.-790T>A (A2M) NP_001334353.1:n.-790T>A
NM_001347425.1:c.-627T>A (A2M) NP_001334354.1:n.-627T>A
XM_017018683.1:c.*34-9188A>T (KLRG1) XP_016874172.1:n.*34-9188A>T
XM_017018684.1:c.*34-18900A>T (KLRG1) XP_016874173.1:n.*34-18900A>T
XM_017018685.1:c.*33+58020A>T (KLRG1) XP_016874174.1:n.*33+58020A>T
NM_001347423.2:c.-76T>A (A2M) NP_001334352.2:n.-76T>A