Canonical Allele Identifier: CA320696008

Gene: FAM3B

Linked Data

• dbSNP Id: rs1037241299
• MyVariant Identifiers: chr21:g.42698858G>A (hg19) ; chr21:g.41326931G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41326931G>A , CM000683.2:g.41326931G>A	GRCh38
NC_000021.8:g.42698858G>A , CM000683.1:g.42698858G>A	GRCh37
NC_000021.7:g.41620728G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357985.7:c.163+3865G>A MANE Select	ENSP00000350673.2:n.163+3865G>A
ENST00000357985.6:c.163+3865G>A	ENSP00000350673.2:n.163+3865G>A
ENST00000398646.3:c.232+3865G>A	ENSP00000381641.3:n.232+3865G>A
ENST00000398647.7:c.19+10033G>A	ENSP00000381642.3:n.19+10033G>A
ENST00000398652.7:c.280+3865G>A	ENSP00000381646.3:n.280+3865G>A
ENST00000479810.6:n.1764+3865G>A
ENST00000518236.1:n.205+3865G>A
NM_058186.3:c.163+3865G>A	NP_478066.3:n.163+3865G>A
NM_206964.1:c.19+10033G>A	NP_996847.1:n.19+10033G>A
XM_011529648.1:c.163+3865G>A	XP_011527950.1:n.163+3865G>A
XM_011529649.1:c.205+3865G>A	XP_011527951.1:n.205+3865G>A
XR_937526.1:n.662+3865G>A
XM_011529648.2:c.391+3865G>A	XP_011527950.2:n.391+3865G>A
XM_011529649.2:c.205+3865G>A	XP_011527951.1:n.205+3865G>A
XR_937526.2:n.663+3865G>A
NM_058186.4:c.163+3865G>A MANE Select	NP_478066.3:n.163+3865G>A
NM_206964.2:c.19+10033G>A	NP_996847.1:n.19+10033G>A