Canonical Allele Identifier: CA2579268350

Gene: CYP11B2 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142912451C>T , CM000670.2:g.142912451C>T	GRCh38
NC_000008.10:g.143993867C>T , CM000670.1:g.143993867C>T	GRCh37
NC_000008.9:g.143990869C>T	NCBI36
NG_008374.1:g.10393G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000323110.2:c.1398+79G>A (CYP11B2) MANE Select	ENSP00000325822.2:n.1398+79G>A
ENST00000522728.5:c.182-1512C>T (GML)	ENSP00000430799.1:n.182-1512C>T
NM_000498.3:c.1398+79G>A (CYP11B2) MANE Select	NP_000489.3:n.1398+79G>A
XM_011516877.1:c.1545+79G>A (CYP11B2)	XP_011515179.1:n.1545+79G>A
XM_011516878.1:c.1476+79G>A (CYP11B2)	XP_011515180.1:n.1476+79G>A
XM_011516879.1:c.1467+79G>A (CYP11B2)	XP_011515181.1:n.1467+79G>A
XM_011516970.1:c.215-1512C>T (GML)	XP_011515272.1:n.215-1512C>T