Canonical Allele Identifier: CA1825515559
Gene: CYP11B2 HGNC NCBI
GML HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142914450C= , CM000670.2:g.142914450C= GRCh38
NC_000008.10:g.143995866C= , CM000670.1:g.143995866C= GRCh37
NC_000008.9:g.143992868C= NCBI36
NG_008374.1:g.8394G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323110.2:c.800-32G= (CYP11B2) MANE Select ENSP00000325822.2:n.800-32G=
ENST00000522728.5:c.264+405C= (GML) ENSP00000430799.1:n.264+405C=
NM_000498.3:c.800-32G= (CYP11B2) MANE Select NP_000489.3:n.800-32G=
XM_011516877.1:c.878-32G= (CYP11B2) XP_011515179.1:n.878-32G=
XM_011516878.1:c.878-32G= (CYP11B2) XP_011515180.1:n.878-32G=
XM_011516879.1:c.800-32G= (CYP11B2) XP_011515181.1:n.800-32G=
XM_011516970.1:c.297+405C= (GML) XP_011515272.1:n.297+405C=
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