Canonical Allele Identifier: CA372389082

Linked Data

dbSNP Id: rs2130329698

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142914707T>C , CM000670.2:g.142914707T>C GRCh38
NC_000008.10:g.143996123T>C , CM000670.1:g.143996123T>C GRCh37
NC_000008.9:g.143993125T>C NCBI36
NG_008374.1:g.8137A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323110.2:c.797A>G (CYP11B2) MANE Select ENSP00000325822.2:p.Tyr266Cys
ENST00000522728.5:c.264+662T>C (GML) ENSP00000430799.1:n.264+662T>C
NM_000498.3:c.797A>G (CYP11B2) MANE Select NP_000489.3:p.Tyr266Cys
XM_011516877.1:c.875A>G (CYP11B2) XP_011515179.1:p.Tyr292Cys
XM_011516878.1:c.875A>G (CYP11B2) XP_011515180.1:p.Tyr292Cys
XM_011516879.1:c.797A>G (CYP11B2) XP_011515181.1:p.Tyr266Cys
XM_011516970.1:c.297+662T>C (GML) XP_011515272.1:n.297+662T>C