Canonical Allele Identifier: CA1441689233

Gene: FAM184B

Linked Data

• dbSNP Id: rs1716424618

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17681203_17681204insTACCTTTGGTACCTTTGG , CM000666.2:g.17681203_17681204insTACCTTTGGTACCTTTGG	GRCh38
NC_000004.11:g.17682826_17682827insTACCTTTGGTACCTTTGG , CM000666.1:g.17682826_17682827insTACCTTTGGTACCTTTGG	GRCh37
NC_000004.10:g.17291924_17291925insTACCTTTGGTACCTTTGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265018.4:c.1596+7227_1596+7228insTACCAAAGGTACCAAAGG MANE Select	ENSP00000265018.3:n.1596+7227_1596+7228insTACCAAAGGTACCAAAGG
ENST00000265018.3:c.1596+7227_1596+7228insTACCAAAGGTACCAAAGG	ENSP00000265018.3:n.1596+7227_1596+7228insTACCAAAGGTACCAAAGG
NM_015688.1:c.1596+7227_1596+7228insTACCAAAGGTACCAAAGG	NP_056503.1:n.1596+7227_1596+7228insTACCAAAGGTACCAAAGG
XM_011513834.1:c.1596+7227_1596+7228insTACCAAAGGTACCAAAGG	XP_011512136.1:n.1596+7227_1596+7228insTACCAAAGGTACCAAAGG
NM_015688.2:c.1596+7227_1596+7228insTACCAAAGGTACCAAAGG MANE Select	NP_056503.1:n.1596+7227_1596+7228insTACCAAAGGTACCAAAGG