Canonical Allele Identifier: CA372389122

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142914723C>A , CM000670.2:g.142914723C>A GRCh38
NC_000008.10:g.143996139C>A , CM000670.1:g.143996139C>A GRCh37
NC_000008.9:g.143993141C>A NCBI36
NG_008374.1:g.8121G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000323110.2:c.781G>T (CYP11B2) MANE Select ENSP00000325822.2:p.Asp261Tyr
ENST00000522728.5:c.264+678C>A (GML) ENSP00000430799.1:n.264+678C>A
NM_000498.3:c.781G>T (CYP11B2) MANE Select NP_000489.3:p.Asp261Tyr
XM_011516877.1:c.859G>T (CYP11B2) XP_011515179.1:p.Asp287Tyr
XM_011516878.1:c.859G>T (CYP11B2) XP_011515180.1:p.Asp287Tyr
XM_011516879.1:c.781G>T (CYP11B2) XP_011515181.1:p.Asp261Tyr
XM_011516970.1:c.297+678C>A (GML) XP_011515272.1:n.297+678C>A