Canonical Allele Identifier: CA1825515425

Gene: CYP11B2 GML

Linked Data

• dbSNP Id: rs1817594216

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142914206T>A , CM000670.2:g.142914206T>A	GRCh38
NC_000008.10:g.143995622T>A , CM000670.1:g.143995622T>A	GRCh37
NC_000008.9:g.143992624T>A	NCBI36
NG_008374.1:g.8638A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323110.2:c.954+58A>T (CYP11B2) MANE Select	ENSP00000325822.2:n.954+58A>T
ENST00000522728.5:c.264+161T>A (GML)	ENSP00000430799.1:n.264+161T>A
NM_000498.3:c.954+58A>T (CYP11B2) MANE Select	NP_000489.3:n.954+58A>T
XM_011516877.1:c.1032+58A>T (CYP11B2)	XP_011515179.1:n.1032+58A>T
XM_011516878.1:c.1032+58A>T (CYP11B2)	XP_011515180.1:n.1032+58A>T
XM_011516879.1:c.954+58A>T (CYP11B2)	XP_011515181.1:n.954+58A>T
XM_011516970.1:c.297+161T>A (GML)	XP_011515272.1:n.297+161T>A