Canonical Allele Identifier: CA1441689196
Gene: FAM184B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681102G= , CM000666.2:g.17681102G= GRCh38
NC_000004.11:g.17682725G= , CM000666.1:g.17682725G= GRCh37
NC_000004.10:g.17291823G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265018.4:c.1596+7322C= MANE Select ENSP00000265018.3:n.1596+7322C=
ENST00000265018.3:c.1596+7322C= ENSP00000265018.3:n.1596+7322C=
NM_015688.1:c.1596+7322C= NP_056503.1:n.1596+7322C=
XM_011513834.1:c.1596+7322C= XP_011512136.1:n.1596+7322C=
NM_015688.2:c.1596+7322C= MANE Select NP_056503.1:n.1596+7322C=