Canonical Allele Identifier: CA1825514067

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142911828C= , CM000670.2:g.142911828C= GRCh38
NC_000008.10:g.143993244C= , CM000670.1:g.143993244C= GRCh37
NC_000008.9:g.143990246C= NCBI36
NG_008374.1:g.11016G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323110.2:c.*152G= (CYP11B2) MANE Select ENSP00000325822.2:n.*152G=
ENST00000522728.5:c.182-2135C= (GML) ENSP00000430799.1:n.182-2135C=
NM_000498.3:c.*152G= (CYP11B2) MANE Select NP_000489.3:n.*152G=
XM_011516877.1:c.*152G= (CYP11B2) XP_011515179.1:n.*152G=
XM_011516878.1:c.*152G= (CYP11B2) XP_011515180.1:n.*152G=
XM_011516879.1:c.*152G= (CYP11B2) XP_011515181.1:n.*152G=
XM_011516970.1:c.215-2135C= (GML) XP_011515272.1:n.215-2135C=