Canonical Allele Identifier: CA6438333

Identifiers and link-outs to other resources

dbSNP Id: rs11609582

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9090027A>T , CM000674.2:g.9090027A>T GRCh38
NC_000012.11:g.9242623A>T , CM000674.1:g.9242623A>T GRCh37
NC_000012.10:g.9133890A>T NCBI36
NG_011717.1:g.30936T>A

Transcript Alleles

HGVS Amino-acid change
NM_000014.4:c.2597-4T>A (A2M) VV NP_000005.2:p.=
XM_006719056.2:c.2597-4T>A (A2M) XP_006719119.1:p.=
NM_000014.5:c.2597-4T>A (A2M) VV
NM_001347423.1:c.2597-4T>A (A2M) VV NP_001334352.1:p.=
NM_001347424.1:c.2297-4T>A (A2M) VV NP_001334353.1:p.=
NM_001347425.1:c.2147-4T>A (A2M) VV NP_001334354.1:p.=
XM_006719056.3:c.2597-4T>A (A2M)
XM_017018683.1:c.*33+31861A>T (KLRG1) XP_016874172.1:p.=
XM_017018684.1:c.*33+31861A>T (KLRG1) XP_016874173.1:p.=
XM_017018685.1:c.*33+31861A>T (KLRG1) XP_016874174.1:p.=
ENST00000318602.11:c.2597-4T>A ENSP00000323929.7:p.=
ENST00000462568.1:n.176-4T>A
ENST00000543436.2:n.340-4T>A
ENST00000545828.1:n.348+11523T>A