Canonical Allele Identifier: CA93291731
Gene: FAM184B HGNC NCBI

Linked Data

dbSNP Id: rs986627243
MyVariant Identifiers: chr4:g.17682643C>T (hg19) chr4:g.17681020C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681020C>T , CM000666.2:g.17681020C>T GRCh38
NC_000004.11:g.17682643C>T , CM000666.1:g.17682643C>T GRCh37
NC_000004.10:g.17291741C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265018.4:c.1596+7404G>A MANE Select ENSP00000265018.3:n.1596+7404G>A
ENST00000265018.3:c.1596+7404G>A ENSP00000265018.3:n.1596+7404G>A
NM_015688.1:c.1596+7404G>A NP_056503.1:n.1596+7404G>A
XM_011513834.1:c.1596+7404G>A XP_011512136.1:n.1596+7404G>A
NM_015688.2:c.1596+7404G>A MANE Select NP_056503.1:n.1596+7404G>A
Search 100 bp 5'
Search 100 bp 3'