Canonical Allele Identifier: CA372389077

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142914705C>G , CM000670.2:g.142914705C>G GRCh38
NC_000008.10:g.143996121C>G , CM000670.1:g.143996121C>G GRCh37
NC_000008.9:g.143993123C>G NCBI36
NG_008374.1:g.8139G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000323110.2:c.799G>C (CYP11B2) MANE Select ENSP00000325822.2:p.Gly267Arg
ENST00000522728.5:c.264+660C>G (GML) ENSP00000430799.1:n.264+660C>G
NM_000498.3:c.799G>C (CYP11B2) MANE Select NP_000489.3:p.Gly267Arg
XM_011516877.1:c.877G>C (CYP11B2) XP_011515179.1:p.Gly293Arg
XM_011516878.1:c.877G>C (CYP11B2) XP_011515180.1:p.Gly293Arg
XM_011516879.1:c.799G>C (CYP11B2) XP_011515181.1:p.Gly267Arg
XM_011516970.1:c.297+660C>G (GML) XP_011515272.1:n.297+660C>G