Canonical Allele Identifier: CA1441689164
Gene: FAM184B HGNC NCBI

Linked Data

dbSNP Id: rs1716421876

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681019A>C , CM000666.2:g.17681019A>C GRCh38
NC_000004.11:g.17682642A>C , CM000666.1:g.17682642A>C GRCh37
NC_000004.10:g.17291740A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265018.4:c.1596+7405T>G MANE Select ENSP00000265018.3:n.1596+7405T>G
ENST00000265018.3:c.1596+7405T>G ENSP00000265018.3:n.1596+7405T>G
NM_015688.1:c.1596+7405T>G NP_056503.1:n.1596+7405T>G
XM_011513834.1:c.1596+7405T>G XP_011512136.1:n.1596+7405T>G
NM_015688.2:c.1596+7405T>G MANE Select NP_056503.1:n.1596+7405T>G