Canonical Allele Identifier: CA603222318

Linked Data

dbSNP Id: rs1451992872
gnomAD v2: 12-9242624-A-T
gnomAD v3: 12-9090028-A-T
gnomAD v4: 12-9090028-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9090028A>T , CM000674.2:g.9090028A>T GRCh38
NC_000012.11:g.9242624A>T , CM000674.1:g.9242624A>T GRCh37
NC_000012.10:g.9133891A>T NCBI36
NG_011717.1:g.30935T>A
NG_011717.2:g.30935T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000318602.12:c.2597-5T>A (A2M) MANE Select ENSP00000323929.8:n.2597-5T>A
ENST00000318602.11:c.2597-5T>A (A2M) ENSP00000323929.7:n.2597-5T>A
ENST00000462568.1:n.176-5T>A (A2M)
ENST00000543436.2:n.340-5T>A (A2M)
ENST00000545828.1:n.348+11522T>A (A2M)
NM_000014.4:c.2597-5T>A (A2M) NP_000005.2:n.2597-5T>A
XM_006719056.2:c.2597-5T>A (A2M) XP_006719119.1:n.2597-5T>A
NM_000014.5:c.2597-5T>A (A2M) NP_000005.2:n.2597-5T>A
NM_001347423.1:c.2597-5T>A (A2M) NP_001334352.1:n.2597-5T>A
NM_001347424.1:c.2297-5T>A (A2M) NP_001334353.1:n.2297-5T>A
NM_001347425.1:c.2147-5T>A (A2M) NP_001334354.1:n.2147-5T>A
XM_006719056.3:c.2597-5T>A (A2M) XP_006719119.1:n.2597-5T>A
XM_017018683.1:c.*33+31862A>T (KLRG1) XP_016874172.1:n.*33+31862A>T
XM_017018684.1:c.*33+31862A>T (KLRG1) XP_016874173.1:n.*33+31862A>T
XM_017018685.1:c.*33+31862A>T (KLRG1) XP_016874174.1:n.*33+31862A>T
NM_000014.6:c.2597-5T>A (A2M) MANE Select NP_000005.3:n.2597-5T>A
NM_001347423.2:c.2597-5T>A (A2M) NP_001334352.2:n.2597-5T>A
NM_001347424.2:c.2297-5T>A (A2M) NP_001334353.2:n.2297-5T>A
NM_001347425.2:c.2147-5T>A (A2M) NP_001334354.2:n.2147-5T>A