Canonical Allele Identifier: CA463332221

Linked Data

MyVariant Identifiers: chr8:g.143996155C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142914739C>T , CM000670.2:g.142914739C>T GRCh38
NC_000008.10:g.143996155C>T , CM000670.1:g.143996155C>T GRCh37
NC_000008.9:g.143993157C>T NCBI36
NG_008374.1:g.8105G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000323110.2:c.765G>A (CYP11B2) MANE Select ENSP00000325822.2:p.Glu255=
ENST00000522728.5:c.264+694C>T (GML) ENSP00000430799.1:n.264+694C>T
NM_000498.3:c.765G>A (CYP11B2) MANE Select NP_000489.3:p.Glu255=
XM_011516877.1:c.843G>A (CYP11B2) XP_011515179.1:p.Glu281=
XM_011516878.1:c.843G>A (CYP11B2) XP_011515180.1:p.Glu281=
XM_011516879.1:c.765G>A (CYP11B2) XP_011515181.1:p.Glu255=
XM_011516970.1:c.297+694C>T (GML) XP_011515272.1:n.297+694C>T