Canonical Allele Identifier: CA187452879

Linked Data

dbSNP Id: rs1009894155

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142911920C>T , CM000670.2:g.142911920C>T GRCh38
NC_000008.10:g.143993336C>T , CM000670.1:g.143993336C>T GRCh37
NC_000008.9:g.143990338C>T NCBI36
NG_008374.1:g.10924G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.*60G>A (CYP11B2) MANE Select ENSP00000325822.2:n.*60G>A
ENST00000522728.5:c.182-2043C>T (GML) ENSP00000430799.1:n.182-2043C>T
NM_000498.3:c.*60G>A (CYP11B2) MANE Select NP_000489.3:n.*60G>A
XM_011516877.1:c.*60G>A (CYP11B2) XP_011515179.1:n.*60G>A
XM_011516878.1:c.*60G>A (CYP11B2) XP_011515180.1:n.*60G>A
XM_011516879.1:c.*60G>A (CYP11B2) XP_011515181.1:n.*60G>A
XM_011516970.1:c.215-2043C>T (GML) XP_011515272.1:n.215-2043C>T