Canonical Allele Identifier: CA10708189
Gene: FMN2 HGNC NCBI

Linked Data

dbSNP Id: rs9662388
gnomAD v2: 1-240552223-G-A
gnomAD v3: 1-240388923-G-A
gnomAD v4: 1-240388923-G-A
MyVariant Identifiers: chr1:g.240552223G>A (hg19) chr1:g.240388923G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240388923G>A , CM000663.2:g.240388923G>A GRCh38
NC_000001.10:g.240552223G>A , CM000663.1:g.240552223G>A GRCh37
NC_000001.9:g.238618846G>A NCBI36
NG_042054.1:g.302039G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000319653.14:c.4859-3588G>A MANE Select ENSP00000318884.9:n.4859-3588G>A
ENST00000545751.3:c.700-3588G>A
ENST00000679390.1:n.1121-3588G>A
ENST00000679646.1:n.4325-3588G>A
ENST00000679980.1:c.1128-3588G>A
ENST00000681131.1:c.859-3588G>A
ENST00000681210.1:c.1079-3588G>A ENSP00000505131.1:n.1079-3588G>A
ENST00000681296.1:n.2046-3588G>A
ENST00000681741.1:c.*903-3588G>A ENSP00000505116.1:n.*903-3588G>A
ENST00000681805.1:c.744-3588G>A
ENST00000681824.1:c.986-3588G>A ENSP00000505818.1:n.986-3588G>A
ENST00000319653.13:c.4859-3588G>A ENSP00000318884.9:n.4859-3588G>A
ENST00000545751.2:c.287-3588G>A ENSP00000437918.2:n.287-3588G>A
NM_001305424.1:c.4871-3588G>A NP_001292353.1:n.4871-3588G>A
NM_020066.4:c.4859-3588G>A NP_064450.3:n.4859-3588G>A
NM_001348094.1:c.2687-3588G>A NP_001335023.1:n.2687-3588G>A
XM_017001840.2:c.2999-3588G>A XP_016857329.1:n.2999-3588G>A
XM_017001841.2:c.2999-3588G>A XP_016857330.1:n.2999-3588G>A
NM_020066.5:c.4859-3588G>A MANE Select NP_064450.3:n.4859-3588G>A
NM_001305424.2:c.4871-3588G>A NP_001292353.1:n.4871-3588G>A
NM_001348094.2:c.2687-3588G>A NP_001335023.1:n.2687-3588G>A
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