Canonical Allele Identifier: CA73678347

Gene: FYCO1

Linked Data

• ClinVar Variation Id: 1182251
• ClinVar RCV Id: RCV001539839
• dbSNP Id: rs34786605
• gnomAD v2: 3-46005573-C-G
• gnomAD v3: 3-45964081-C-G
• gnomAD v4: 3-45964081-C-G
• MyVariant Identifiers: chr3:g.46005573C>G (hg19) ; chr3:g.45964081C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45964081C>G , CM000665.2:g.45964081C>G	GRCh38
NC_000003.11:g.46005573C>G , CM000665.1:g.46005573C>G	GRCh37
NC_000003.10:g.45980577C>G	NCBI36
NG_031955.1:g.36744G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296137.7:c.3269+255G>C MANE Select	ENSP00000296137.2:n.3269+255G>C
ENST00000296137.6:c.3269+255G>C	ENSP00000296137.2:n.3269+255G>C
ENST00000535325.5:c.3269+255G>C	ENSP00000441178.1:n.3269+255G>C
NM_024513.3:c.3269+255G>C	NP_078789.2:n.3269+255G>C
XM_006713333.2:c.3269+255G>C	XP_006713396.1:n.3269+255G>C
XM_006713334.2:c.3269+255G>C	XP_006713397.1:n.3269+255G>C
XM_011534111.1:c.3269+255G>C	XP_011532413.1:n.3269+255G>C
XM_011534112.1:c.3269+255G>C	XP_011532414.1:n.3269+255G>C
XR_245157.1:n.3484+255G>C
XM_006713333.3:c.3269+255G>C	XP_006713396.1:n.3269+255G>C
XM_006713334.3:c.3269+255G>C	XP_006713397.1:n.3269+255G>C
XM_011534111.3:c.3269+255G>C	XP_011532413.1:n.3269+255G>C
XR_001740265.1:n.3365+952G>C
NM_024513.4:c.3269+255G>C MANE Select	NP_078789.2:n.3269+255G>C
NM_001386421.1:c.3269+255G>C	NP_001373350.1:n.3269+255G>C
NM_001386422.1:c.3269+255G>C	NP_001373351.1:n.3269+255G>C
NM_001386423.1:c.3269+255G>C	NP_001373352.1:n.3269+255G>C
NM_001386424.1:c.3269+255G>C	NP_001373353.1:n.3269+255G>C
NM_001386425.1:c.3269+255G>C	NP_001373354.1:n.3269+255G>C
NM_001386426.1:c.3149+255G>C	NP_001373355.1:n.3149+255G>C
NM_001386427.1:c.3125+255G>C	NP_001373356.1:n.3125+255G>C
NM_001386428.1:c.3269+255G>C	NP_001373357.1:n.3269+255G>C
NM_001386429.1:c.3269+255G>C	NP_001373358.1:n.3269+255G>C
NM_001386430.1:c.2669+255G>C	NP_001373359.1:n.2669+255G>C
NR_170107.1:n.3484+255G>C