Canonical Allele Identifier: CA10627706

Gene: FANCC

Linked Data

• ClinVar Variation Id: 367611
• ClinVar RCV Id: RCV000309313 ; RCV000503247 ; RCV000830234
• dbSNP Id: rs549658720
• gnomAD v2: 9-98079884-T-G
• gnomAD v3: 9-95317602-T-G
• gnomAD v4: 9-95317602-T-G
• MyVariant Identifiers: chr9:g.98079884T>G (hg19) ; chr9:g.95317602T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95317602T>G , CM000671.2:g.95317602T>G	GRCh38
NC_000009.11:g.98079884T>G , CM000671.1:g.98079884T>G	GRCh37
NC_000009.10:g.97119705T>G	NCBI36
NG_011707.1:g.5108A>C , LRG_497:g.5108A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.92A>C
ENST00000696262.1:c.-155A>C	ENSP00000512510.1:n.-155A>C
ENST00000696263.1:n.101A>C
ENST00000289081.8:c.-155A>C MANE Select	ENSP00000289081.3:n.-155A>C
ENST00000490972.7:c.-155A>C	ENSP00000479931.1:n.-155A>C
ENST00000636777.1:n.20-68272A>C
ENST00000647778.1:c.-269A>C	ENSP00000498125.1:n.-269A>C
ENST00000649611.1:c.-314A>C	ENSP00000497986.1:n.-314A>C
ENST00000289081.7:c.-155A>C	ENSP00000289081.3:n.-155A>C
ENST00000474949.1:n.108A>C
ENST00000490972.6:c.-155A>C	ENSP00000479931.1:n.-155A>C
NM_000136.2:c.-155A>C , LRG_497t1:c.-155A>C	NP_000127.2:n.-155A>C
NM_001243744.1:c.-155A>C	NP_001230673.1:n.-155A>C
XM_006717001.1:c.-155A>C	XP_006717064.1:n.-155A>C
XM_006717002.2:c.-155A>C	XP_006717065.1:n.-155A>C
XM_006717004.2:c.-155A>C	XP_006717067.1:n.-155A>C
XM_011518366.1:c.-155A>C	XP_011516668.1:n.-155A>C
XM_006717001.3:c.-155A>C	XP_006717064.1:n.-155A>C
XM_006717002.4:c.-155A>C	XP_006717065.1:n.-155A>C
XM_006717004.4:c.-155A>C	XP_006717067.1:n.-155A>C
XM_011518366.3:c.-155A>C	XP_011516668.1:n.-155A>C
XM_017014452.2:c.-756A>C	XP_016869941.1:n.-756A>C
XM_017014454.1:c.-756A>C	XP_016869943.1:n.-756A>C
NM_000136.3:c.-155A>C MANE Select	NP_000127.2:n.-155A>C
NM_001243744.2:c.-155A>C	NP_001230673.1:n.-155A>C