Canonical Allele Identifier: CA1441689189
Gene: FAM184B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681085C= , CM000666.2:g.17681085C= GRCh38
NC_000004.11:g.17682708C= , CM000666.1:g.17682708C= GRCh37
NC_000004.10:g.17291806C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265018.4:c.1596+7339G= MANE Select ENSP00000265018.3:n.1596+7339G=
ENST00000265018.3:c.1596+7339G= ENSP00000265018.3:n.1596+7339G=
NM_015688.1:c.1596+7339G= NP_056503.1:n.1596+7339G=
XM_011513834.1:c.1596+7339G= XP_011512136.1:n.1596+7339G=
NM_015688.2:c.1596+7339G= MANE Select NP_056503.1:n.1596+7339G=
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