Canonical Allele Identifier: CA1982223118

Gene: FCHSD2

Linked Data

• dbSNP Id: rs1856787649

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72959782A>T , CM000673.2:g.72959782A>T	GRCh38
NC_000011.9:g.72670827A>T , CM000673.1:g.72670827A>T	GRCh37
NC_000011.8:g.72348475A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409418.9:c.705+24306T>A MANE Select	ENSP00000386722.4:n.705+24306T>A
ENST00000311172.11:c.537+24306T>A	ENSP00000308978.7:n.537+24306T>A
ENST00000409314.5:c.705+24306T>A	ENSP00000386987.1:n.705+24306T>A
ENST00000409418.8:c.705+24306T>A	ENSP00000386722.4:n.705+24306T>A
ENST00000409853.5:c.537+24306T>A	ENSP00000386314.1:n.537+24306T>A
ENST00000458644.6:c.225+24306T>A	ENSP00000402972.2:n.225+24306T>A
NM_014824.2:c.705+24306T>A	NP_055639.2:n.705+24306T>A
XM_011545409.1:c.642+24306T>A	XP_011543711.1:n.642+24306T>A
XM_011545410.1:c.630+24306T>A	XP_011543712.1:n.630+24306T>A
XM_011545411.1:c.471+24306T>A	XP_011543713.1:n.471+24306T>A
XM_011545412.1:c.705+24306T>A	XP_011543714.1:n.705+24306T>A
XM_011545410.2:c.630+24306T>A	XP_011543712.1:n.630+24306T>A
XM_017018632.1:c.642+24306T>A	XP_016874121.1:n.642+24306T>A
XR_001748055.1:n.1510+24306T>A
NM_014824.3:c.705+24306T>A MANE Select	NP_055639.2:n.705+24306T>A