Canonical Allele Identifier: CA1441689252
Gene: FAM184B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681230T= , CM000666.2:g.17681230T= GRCh38
NC_000004.11:g.17682853T= , CM000666.1:g.17682853T= GRCh37
NC_000004.10:g.17291951T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265018.4:c.1596+7194A= MANE Select ENSP00000265018.3:n.1596+7194A=
ENST00000265018.3:c.1596+7194A= ENSP00000265018.3:n.1596+7194A=
NM_015688.1:c.1596+7194A= NP_056503.1:n.1596+7194A=
XM_011513834.1:c.1596+7194A= XP_011512136.1:n.1596+7194A=
NM_015688.2:c.1596+7194A= MANE Select NP_056503.1:n.1596+7194A=
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