Canonical Allele Identifier: CA2794496560

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9116077A>T , CM000674.2:g.9116077A>T GRCh38
NC_000012.11:g.9268673A>T , CM000674.1:g.9268673A>T GRCh37
NC_000012.10:g.9159940A>T NCBI36
NG_011717.1:g.4886T>A
NG_011717.2:g.4886T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318602.11:c.-228T>A (A2M) ENSP00000323929.7:n.-228T>A
ENST00000404455.2:c.-18+51T>A (A2M) ENSP00000385710.2:n.-18+51T>A
NM_000014.5:c.-228T>A (A2M) NP_000005.2:n.-228T>A
NM_001347423.1:c.-18+51T>A (A2M) NP_001334352.1:n.-18+51T>A
NM_001347424.1:c.-681T>A (A2M) NP_001334353.1:n.-681T>A
NM_001347425.1:c.-518T>A (A2M) NP_001334354.1:n.-518T>A
XM_017018683.1:c.*34-9297A>T (KLRG1) XP_016874172.1:n.*34-9297A>T
XM_017018684.1:c.*34-19009A>T (KLRG1) XP_016874173.1:n.*34-19009A>T
XM_017018685.1:c.*33+57911A>T (KLRG1) XP_016874174.1:n.*33+57911A>T
NM_001347423.2:c.-18+51T>A (A2M) NP_001334352.2:n.-18+51T>A