Canonical Allele Identifier: CA372385929

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142912548C>T , CM000670.2:g.142912548C>T GRCh38
NC_000008.10:g.143993964C>T , CM000670.1:g.143993964C>T GRCh37
NC_000008.9:g.143990966C>T NCBI36
NG_008374.1:g.10296G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.1380G>A (CYP11B2) MANE Select ENSP00000325822.2:p.Met460Ile
ENST00000522728.5:c.182-1415C>T (GML) ENSP00000430799.1:n.182-1415C>T
NM_000498.3:c.1380G>A (CYP11B2) MANE Select NP_000489.3:p.Met460Ile
XM_011516877.1:c.1527G>A (CYP11B2) XP_011515179.1:p.Met509Ile
XM_011516878.1:c.1458G>A (CYP11B2) XP_011515180.1:p.Met486Ile
XM_011516879.1:c.1449G>A (CYP11B2) XP_011515181.1:p.Met483Ile
XM_011516970.1:c.215-1415C>T (GML) XP_011515272.1:n.215-1415C>T