Canonical Allele Identifier: CA2390271107
Gene: FAM3B HGNC NCBI

Linked Data

dbSNP Id: rs1601355405

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41327098T>C , CM000683.2:g.41327098T>C GRCh38
NC_000021.8:g.42699025T>C , CM000683.1:g.42699025T>C GRCh37
NC_000021.7:g.41620895T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357985.7:c.163+4032T>C MANE Select ENSP00000350673.2:n.163+4032T>C
ENST00000357985.6:c.163+4032T>C ENSP00000350673.2:n.163+4032T>C
ENST00000398646.3:c.232+4032T>C ENSP00000381641.3:n.232+4032T>C
ENST00000398647.7:c.19+10200T>C ENSP00000381642.3:n.19+10200T>C
ENST00000398652.7:c.280+4032T>C ENSP00000381646.3:n.280+4032T>C
ENST00000479810.6:n.1764+4032T>C
ENST00000518236.1:n.205+4032T>C
NM_058186.3:c.163+4032T>C NP_478066.3:n.163+4032T>C
NM_206964.1:c.19+10200T>C NP_996847.1:n.19+10200T>C
XM_011529648.1:c.163+4032T>C XP_011527950.1:n.163+4032T>C
XM_011529649.1:c.205+4032T>C XP_011527951.1:n.205+4032T>C
XR_937526.1:n.662+4032T>C
XM_011529648.2:c.391+4032T>C XP_011527950.2:n.391+4032T>C
XM_011529649.2:c.205+4032T>C XP_011527951.1:n.205+4032T>C
XR_937526.2:n.663+4032T>C
NM_058186.4:c.163+4032T>C MANE Select NP_478066.3:n.163+4032T>C
NM_206964.2:c.19+10200T>C NP_996847.1:n.19+10200T>C