Canonical Allele Identifier: CA1441689199
Gene: FAM184B HGNC NCBI

Linked Data

dbSNP Id: rs1716423262

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681103T>G , CM000666.2:g.17681103T>G GRCh38
NC_000004.11:g.17682726T>G , CM000666.1:g.17682726T>G GRCh37
NC_000004.10:g.17291824T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265018.4:c.1596+7321A>C MANE Select ENSP00000265018.3:n.1596+7321A>C
ENST00000265018.3:c.1596+7321A>C ENSP00000265018.3:n.1596+7321A>C
NM_015688.1:c.1596+7321A>C NP_056503.1:n.1596+7321A>C
XM_011513834.1:c.1596+7321A>C XP_011512136.1:n.1596+7321A>C
NM_015688.2:c.1596+7321A>C MANE Select NP_056503.1:n.1596+7321A>C