Canonical Allele Identifier: CA853606489

Gene: FAM110B

Linked Data

• dbSNP Id: rs1295047945
• MyVariant Identifiers: chr8:g.58986408G>A (hg19) ; chr8:g.58073849G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.58073849G>A , CM000670.2:g.58073849G>A	GRCh38
NC_000008.10:g.58986408G>A , CM000670.1:g.58986408G>A	GRCh37
NC_000008.9:g.59148962G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000519262.6:c.-413-1686G>A MANE Select	ENSP00000509301.1:n.-413-1686G>A
ENST00000361488.7:c.-413-1686G>A	ENSP00000355204.3:n.-413-1686G>A
ENST00000518427.5:n.182-1686G>A
ENST00000519262.5:n.397-1686G>A
ENST00000520369.5:n.338-1686G>A
ENST00000521413.1:n.46-1686G>A
ENST00000522059.5:n.89-1686G>A
ENST00000523486.5:n.137-1686G>A
NM_147189.2:c.-413-1686G>A	NP_671722.1:n.-413-1686G>A
XM_005251324.1:c.-413-1686G>A	XP_005251381.1:n.-413-1686G>A
XM_005251325.2:c.-413-1686G>A	XP_005251382.1:n.-413-1686G>A
XM_005251326.1:c.-413-1686G>A	XP_005251383.1:n.-413-1686G>A
XM_005251324.3:c.-413-1686G>A	XP_005251381.1:n.-413-1686G>A
XM_005251325.3:c.-413-1686G>A	XP_005251382.1:n.-413-1686G>A
XM_005251326.3:c.-413-1686G>A	XP_005251383.1:n.-413-1686G>A
XM_017013948.1:c.-413-1686G>A	XP_016869437.1:n.-413-1686G>A
NM_147189.3:c.-413-1686G>A	NP_671722.1:n.-413-1686G>A
NM_001377989.1:c.-413-1686G>A MANE Select	NP_001364918.1:n.-413-1686G>A
NM_001377997.1:c.-413-1686G>A	NP_001364926.1:n.-413-1686G>A
NM_001377998.1:c.-413-1686G>A	NP_001364927.1:n.-413-1686G>A
NM_147189.4:c.-413-1686G>A	NP_671722.1:n.-413-1686G>A