Canonical Allele Identifier: CA4906062

Linked Data

dbSNP Id: rs754048446

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142914409C>T , CM000670.2:g.142914409C>T GRCh38
NC_000008.10:g.143995825C>T , CM000670.1:g.143995825C>T GRCh37
NC_000008.9:g.143992827C>T NCBI36
NG_008374.1:g.8435G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000323110.2:c.809G>A (CYP11B2) MANE Select ENSP00000325822.2:p.Cys270Tyr
ENST00000522728.5:c.264+364C>T (GML) ENSP00000430799.1:n.264+364C>T
NM_000498.3:c.809G>A (CYP11B2) MANE Select NP_000489.3:p.Cys270Tyr
XM_011516877.1:c.887G>A (CYP11B2) XP_011515179.1:p.Cys296Tyr
XM_011516878.1:c.887G>A (CYP11B2) XP_011515180.1:p.Cys296Tyr
XM_011516879.1:c.809G>A (CYP11B2) XP_011515181.1:p.Cys270Tyr
XM_011516970.1:c.297+364C>T (GML) XP_011515272.1:n.297+364C>T