Canonical Allele Identifier: CA1825514382

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142912461G= , CM000670.2:g.142912461G= GRCh38
NC_000008.10:g.143993877G= , CM000670.1:g.143993877G= GRCh37
NC_000008.9:g.143990879G= NCBI36
NG_008374.1:g.10383C=

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.1398+69C= (CYP11B2) MANE Select ENSP00000325822.2:n.1398+69C=
ENST00000522728.5:c.182-1502G= (GML) ENSP00000430799.1:n.182-1502G=
NM_000498.3:c.1398+69C= (CYP11B2) MANE Select NP_000489.3:n.1398+69C=
XM_011516877.1:c.1545+69C= (CYP11B2) XP_011515179.1:n.1545+69C=
XM_011516878.1:c.1476+69C= (CYP11B2) XP_011515180.1:n.1476+69C=
XM_011516879.1:c.1467+69C= (CYP11B2) XP_011515181.1:n.1467+69C=
XM_011516970.1:c.215-1502G= (GML) XP_011515272.1:n.215-1502G=