Canonical Allele Identifier: CA2760596064

Gene: FAM184B

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17681038T>C , CM000666.2:g.17681038T>C	GRCh38
NC_000004.11:g.17682661T>C , CM000666.1:g.17682661T>C	GRCh37
NC_000004.10:g.17291759T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265018.4:c.1596+7386A>G MANE Select	ENSP00000265018.3:n.1596+7386A>G
ENST00000265018.3:c.1596+7386A>G	ENSP00000265018.3:n.1596+7386A>G
NM_015688.1:c.1596+7386A>G	NP_056503.1:n.1596+7386A>G
XM_011513834.1:c.1596+7386A>G	XP_011512136.1:n.1596+7386A>G
NM_015688.2:c.1596+7386A>G MANE Select	NP_056503.1:n.1596+7386A>G