Canonical Allele Identifier: CA1825514375

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142912452A= , CM000670.2:g.142912452A= GRCh38
NC_000008.10:g.143993868A= , CM000670.1:g.143993868A= GRCh37
NC_000008.9:g.143990870A= NCBI36
NG_008374.1:g.10392T=

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.1398+78T= (CYP11B2) MANE Select ENSP00000325822.2:n.1398+78T=
ENST00000522728.5:c.182-1511A= (GML) ENSP00000430799.1:n.182-1511A=
NM_000498.3:c.1398+78T= (CYP11B2) MANE Select NP_000489.3:n.1398+78T=
XM_011516877.1:c.1545+78T= (CYP11B2) XP_011515179.1:n.1545+78T=
XM_011516878.1:c.1476+78T= (CYP11B2) XP_011515180.1:n.1476+78T=
XM_011516879.1:c.1467+78T= (CYP11B2) XP_011515181.1:n.1467+78T=
XM_011516970.1:c.215-1511A= (GML) XP_011515272.1:n.215-1511A=