Canonical Allele Identifier: CA40315286

Gene: FMN2

Linked Data

• dbSNP Id: rs897325531
• gnomAD v2: 1-240540732-T-C
• gnomAD v3: 1-240377432-T-C
• gnomAD v4: 1-240377432-T-C
• MyVariant Identifiers: chr1:g.240540732T>C (hg19) ; chr1:g.240377432T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240377432T>C , CM000663.2:g.240377432T>C	GRCh38
NC_000001.10:g.240540732T>C , CM000663.1:g.240540732T>C	GRCh37
NC_000001.9:g.238607355T>C	NCBI36
NG_042054.1:g.290548T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319653.14:c.4859-15079T>C MANE Select	ENSP00000318884.9:n.4859-15079T>C
ENST00000545751.3:c.700-15079T>C
ENST00000679390.1:n.1121-15079T>C
ENST00000679646.1:n.4325-15079T>C
ENST00000679980.1:c.1128-15079T>C
ENST00000681131.1:c.859-15079T>C
ENST00000681210.1:c.1079-15079T>C	ENSP00000505131.1:n.1079-15079T>C
ENST00000681296.1:n.2046-15079T>C
ENST00000681741.1:c.*903-15079T>C	ENSP00000505116.1:n.*903-15079T>C
ENST00000681805.1:c.744-15079T>C
ENST00000681824.1:c.986-15079T>C	ENSP00000505818.1:n.986-15079T>C
ENST00000319653.13:c.4859-15079T>C	ENSP00000318884.9:n.4859-15079T>C
ENST00000545751.2:c.287-15079T>C	ENSP00000437918.2:n.287-15079T>C
NM_001305424.1:c.4871-15079T>C	NP_001292353.1:n.4871-15079T>C
NM_020066.4:c.4859-15079T>C	NP_064450.3:n.4859-15079T>C
NM_001348094.1:c.2687-15079T>C	NP_001335023.1:n.2687-15079T>C
XM_017001840.2:c.2999-15079T>C	XP_016857329.1:n.2999-15079T>C
XM_017001841.2:c.2999-15079T>C	XP_016857330.1:n.2999-15079T>C
NM_020066.5:c.4859-15079T>C MANE Select	NP_064450.3:n.4859-15079T>C
NM_001305424.2:c.4871-15079T>C	NP_001292353.1:n.4871-15079T>C
NM_001348094.2:c.2687-15079T>C	NP_001335023.1:n.2687-15079T>C