Canonical Allele Identifier: CA530161202

Gene: FMN2

Linked Data

• dbSNP Id: rs1266895109
• gnomAD v2: 1-240540740-A-G
• gnomAD v3: 1-240377440-A-G
• gnomAD v4: 1-240377440-A-G
• MyVariant Identifiers: chr1:g.240540740A>G (hg19) ; chr1:g.240377440A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.240377440A>G , CM000663.2:g.240377440A>G	GRCh38
NC_000001.10:g.240540740A>G , CM000663.1:g.240540740A>G	GRCh37
NC_000001.9:g.238607363A>G	NCBI36
NG_042054.1:g.290556A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319653.14:c.4859-15071A>G MANE Select	ENSP00000318884.9:n.4859-15071A>G
ENST00000545751.3:c.700-15071A>G
ENST00000679390.1:n.1121-15071A>G
ENST00000679646.1:n.4325-15071A>G
ENST00000679980.1:c.1128-15071A>G
ENST00000681131.1:c.859-15071A>G
ENST00000681210.1:c.1079-15071A>G	ENSP00000505131.1:n.1079-15071A>G
ENST00000681296.1:n.2046-15071A>G
ENST00000681741.1:c.*903-15071A>G	ENSP00000505116.1:n.*903-15071A>G
ENST00000681805.1:c.744-15071A>G
ENST00000681824.1:c.986-15071A>G	ENSP00000505818.1:n.986-15071A>G
ENST00000319653.13:c.4859-15071A>G	ENSP00000318884.9:n.4859-15071A>G
ENST00000545751.2:c.287-15071A>G	ENSP00000437918.2:n.287-15071A>G
NM_001305424.1:c.4871-15071A>G	NP_001292353.1:n.4871-15071A>G
NM_020066.4:c.4859-15071A>G	NP_064450.3:n.4859-15071A>G
NM_001348094.1:c.2687-15071A>G	NP_001335023.1:n.2687-15071A>G
XM_017001840.2:c.2999-15071A>G	XP_016857329.1:n.2999-15071A>G
XM_017001841.2:c.2999-15071A>G	XP_016857330.1:n.2999-15071A>G
NM_020066.5:c.4859-15071A>G MANE Select	NP_064450.3:n.4859-15071A>G
NM_001305424.2:c.4871-15071A>G	NP_001292353.1:n.4871-15071A>G
NM_001348094.2:c.2687-15071A>G	NP_001335023.1:n.2687-15071A>G