Canonical Allele Identifier: CA372388338

Gene: CYP11B2 GML

Linked Data

• MyVariant Identifiers: chr8:g.143995678A>G (hg19) ; chr8:g.142914262A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142914262A>G , CM000670.2:g.142914262A>G	GRCh38
NC_000008.10:g.143995678A>G , CM000670.1:g.143995678A>G	GRCh37
NC_000008.9:g.143992680A>G	NCBI36
NG_008374.1:g.8582T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323110.2:c.954+2T>C (CYP11B2) MANE Select	ENSP00000325822.2:n.954+2T>C
ENST00000522728.5:c.264+217A>G (GML)	ENSP00000430799.1:n.264+217A>G
NM_000498.3:c.954+2T>C (CYP11B2) MANE Select	NP_000489.3:n.954+2T>C
XM_011516877.1:c.1032+2T>C (CYP11B2)	XP_011515179.1:n.1032+2T>C
XM_011516878.1:c.1032+2T>C (CYP11B2)	XP_011515180.1:n.1032+2T>C
XM_011516879.1:c.954+2T>C (CYP11B2)	XP_011515181.1:n.954+2T>C
XM_011516970.1:c.297+217A>G (GML)	XP_011515272.1:n.297+217A>G