Canonical Allele Identifier: CA3343118
Gene: NR2F1 HGNC NCBI

Linked Data

dbSNP Id: rs774052702
ExAC: 5:92921008 G / C
gnomAD v2: 5-92921008-G-C
gnomAD v4: 5-93585302-G-C
MyVariant Identifiers: chr5:g.92921008G>C (hg19) chr5:g.93585302G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585302G>C , CM000667.2:g.93585302G>C GRCh38
NC_000005.9:g.92921008G>C , CM000667.1:g.92921008G>C GRCh37
NC_000005.8:g.92946764G>C NCBI36
NG_034119.1:g.6966G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.204G>C ENSP00000481517.1:p.Ser68=
ENST00000327111.8:c.279G>C MANE Select ENSP00000325819.3:p.Ser93=
ENST00000647447.1:c.126G>C ENSP00000495740.1:p.Ser42=
ENST00000327111.7:c.279G>C ENSP00000325819.3:p.Ser93=
ENST00000615873.1:c.204G>C ENSP00000481517.1:p.Ser68=
NM_005654.5:c.279G>C NP_005645.1:p.Ser93=
NM_005654.6:c.279G>C MANE Select NP_005645.1:p.Ser93=
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