Canonical Allele Identifier: CA1441689186
Gene: FAM184B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681073C= , CM000666.2:g.17681073C= GRCh38
NC_000004.11:g.17682696C= , CM000666.1:g.17682696C= GRCh37
NC_000004.10:g.17291794C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265018.4:c.1596+7351G= MANE Select ENSP00000265018.3:n.1596+7351G=
ENST00000265018.3:c.1596+7351G= ENSP00000265018.3:n.1596+7351G=
NM_015688.1:c.1596+7351G= NP_056503.1:n.1596+7351G=
XM_011513834.1:c.1596+7351G= XP_011512136.1:n.1596+7351G=
NM_015688.2:c.1596+7351G= MANE Select NP_056503.1:n.1596+7351G=
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