Canonical Allele Identifier: CA4906080
Gene: CYP11B2 HGNC NCBI
GML HGNC NCBI

Linked Data

dbSNP Id: rs376229202
ExAC: 8:143995867 T / G
gnomAD v2: 8-143995867-T-G
gnomAD v4: 8-142914451-T-G
MyVariant Identifiers: chr8:g.143995867T>G (hg19) chr8:g.142914451T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142914451T>G , CM000670.2:g.142914451T>G GRCh38
NC_000008.10:g.143995867T>G , CM000670.1:g.143995867T>G GRCh37
NC_000008.9:g.143992869T>G NCBI36
NG_008374.1:g.8393A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000323110.2:c.800-33A>C (CYP11B2) MANE Select ENSP00000325822.2:n.800-33A>C
ENST00000522728.5:c.264+406T>G (GML) ENSP00000430799.1:n.264+406T>G
NM_000498.3:c.800-33A>C (CYP11B2) MANE Select NP_000489.3:n.800-33A>C
XM_011516877.1:c.878-33A>C (CYP11B2) XP_011515179.1:n.878-33A>C
XM_011516878.1:c.878-33A>C (CYP11B2) XP_011515180.1:n.878-33A>C
XM_011516879.1:c.800-33A>C (CYP11B2) XP_011515181.1:n.800-33A>C
XM_011516970.1:c.297+406T>G (GML) XP_011515272.1:n.297+406T>G
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