Canonical Allele Identifier: CA372389131

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142914726A>C , CM000670.2:g.142914726A>C GRCh38
NC_000008.10:g.143996142A>C , CM000670.1:g.143996142A>C GRCh37
NC_000008.9:g.143993144A>C NCBI36
NG_008374.1:g.8118T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323110.2:c.778T>G (CYP11B2) MANE Select ENSP00000325822.2:p.Trp260Gly
ENST00000522728.5:c.264+681A>C (GML) ENSP00000430799.1:n.264+681A>C
NM_000498.3:c.778T>G (CYP11B2) MANE Select NP_000489.3:p.Trp260Gly
XM_011516877.1:c.856T>G (CYP11B2) XP_011515179.1:p.Trp286Gly
XM_011516878.1:c.856T>G (CYP11B2) XP_011515180.1:p.Trp286Gly
XM_011516879.1:c.778T>G (CYP11B2) XP_011515181.1:p.Trp260Gly
XM_011516970.1:c.297+681A>C (GML) XP_011515272.1:n.297+681A>C