Canonical Allele Identifier: CA445569993
Gene: NR2F1 HGNC NCBI

Linked Data

dbSNP Id: rs1753212625
gnomAD v4: 5-93585395-C-G
MyVariant Identifiers: chr5:g.92921101C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585395C>G , CM000667.2:g.93585395C>G GRCh38
NC_000005.9:g.92921101C>G , CM000667.1:g.92921101C>G GRCh37
NC_000005.8:g.92946857C>G NCBI36
NG_034119.1:g.7059C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.297C>G ENSP00000481517.1:p.Ala99=
ENST00000327111.8:c.372C>G MANE Select ENSP00000325819.3:p.Ala124=
ENST00000647447.1:c.219C>G ENSP00000495740.1:p.Ala73=
ENST00000327111.7:c.372C>G ENSP00000325819.3:p.Ala124=
ENST00000615873.1:c.297C>G ENSP00000481517.1:p.Ala99=
NM_005654.5:c.372C>G NP_005645.1:p.Ala124=
NM_005654.6:c.372C>G MANE Select NP_005645.1:p.Ala124=
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