Canonical Allele Identifier: CA2760596066
Gene: FAM184B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681096C>A , CM000666.2:g.17681096C>A GRCh38
NC_000004.11:g.17682719C>A , CM000666.1:g.17682719C>A GRCh37
NC_000004.10:g.17291817C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265018.4:c.1596+7328G>T MANE Select ENSP00000265018.3:n.1596+7328G>T
ENST00000265018.3:c.1596+7328G>T ENSP00000265018.3:n.1596+7328G>T
NM_015688.1:c.1596+7328G>T NP_056503.1:n.1596+7328G>T
XM_011513834.1:c.1596+7328G>T XP_011512136.1:n.1596+7328G>T
NM_015688.2:c.1596+7328G>T MANE Select NP_056503.1:n.1596+7328G>T
Search 100 bp 5'
Search 100 bp 3'