Canonical Allele Identifier: CA463505841

Linked Data

MyVariant Identifiers: chr8:g.143993970T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142912554T>A , CM000670.2:g.142912554T>A GRCh38
NC_000008.10:g.143993970T>A , CM000670.1:g.143993970T>A GRCh37
NC_000008.9:g.143990972T>A NCBI36
NG_008374.1:g.10290A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.1374A>T (CYP11B2) MANE Select ENSP00000325822.2:p.Ala458=
ENST00000522728.5:c.182-1409T>A (GML) ENSP00000430799.1:n.182-1409T>A
NM_000498.3:c.1374A>T (CYP11B2) MANE Select NP_000489.3:p.Ala458=
XM_011516877.1:c.1521A>T (CYP11B2) XP_011515179.1:p.Ala507=
XM_011516878.1:c.1452A>T (CYP11B2) XP_011515180.1:p.Ala484=
XM_011516879.1:c.1443A>T (CYP11B2) XP_011515181.1:p.Ala481=
XM_011516970.1:c.215-1409T>A (GML) XP_011515272.1:n.215-1409T>A