Canonical Allele Identifier: CA1825514101

Linked Data

dbSNP Id: rs1340605191

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142911911_142911912insT , CM000670.2:g.142911911_142911912insT GRCh38
NC_000008.10:g.143993327_143993328insT , CM000670.1:g.143993327_143993328insT GRCh37
NC_000008.9:g.143990329_143990330insT NCBI36
NG_008374.1:g.10932_10933insA

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.*68_*69insA (CYP11B2) MANE Select ENSP00000325822.2:n.*68_*69insA
ENST00000522728.5:c.182-2052_182-2051insT (GML) ENSP00000430799.1:n.182-2052_182-2051insT...
NM_000498.3:c.*68_*69insA (CYP11B2) MANE Select NP_000489.3:n.*68_*69insA
XM_011516877.1:c.*68_*69insA (CYP11B2) XP_011515179.1:n.*68_*69insA
XM_011516878.1:c.*68_*69insA (CYP11B2) XP_011515180.1:n.*68_*69insA
XM_011516879.1:c.*68_*69insA (CYP11B2) XP_011515181.1:n.*68_*69insA
XM_011516970.1:c.215-2052_215-2051insT (GML) XP_011515272.1:n.215-2052_215-2051insT