Canonical Allele Identifier: CA1825515656
Gene: CYP11B2 HGNC NCBI
GML HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142914607T= , CM000670.2:g.142914607T= GRCh38
NC_000008.10:g.143996023T= , CM000670.1:g.143996023T= GRCh37
NC_000008.9:g.143993025T= NCBI36
NG_008374.1:g.8237A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323110.2:c.799+98A= (CYP11B2) MANE Select ENSP00000325822.2:n.799+98A=
ENST00000522728.5:c.264+562T= (GML) ENSP00000430799.1:n.264+562T=
NM_000498.3:c.799+98A= (CYP11B2) MANE Select NP_000489.3:n.799+98A=
XM_011516877.1:c.877+98A= (CYP11B2) XP_011515179.1:n.877+98A=
XM_011516878.1:c.877+98A= (CYP11B2) XP_011515180.1:n.877+98A=
XM_011516879.1:c.799+98A= (CYP11B2) XP_011515181.1:n.799+98A=
XM_011516970.1:c.297+562T= (GML) XP_011515272.1:n.297+562T=
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