Canonical Allele Identifier: CA1441689201
Gene: FAM184B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681107_17681108delinsTG , CM000666.2:g.17681107_17681108delinsTG GRCh38
NC_000004.11:g.17682730_17682731delinsTG , CM000666.1:g.17682730_17682731delinsTG GRCh37
NC_000004.10:g.17291828_17291829delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265018.4:c.1596+7316_1596+7317delinsCA MANE Select ENSP00000265018.3:n.1596+7316_1596+7317delinsCA
ENST00000265018.3:c.1596+7316_1596+7317delinsCA ENSP00000265018.3:n.1596+7316_1596+7317delinsCA
NM_015688.1:c.1596+7316_1596+7317delinsCA NP_056503.1:n.1596+7316_1596+7317delinsCA
XM_011513834.1:c.1596+7316_1596+7317delinsCA XP_011512136.1:n.1596+7316_1596+7317delinsCA
NM_015688.2:c.1596+7316_1596+7317delinsCA MANE Select NP_056503.1:n.1596+7316_1596+7317delinsCA
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