Canonical Allele Identifier: CA445722147
Gene: NR2F1 HGNC NCBI

Linked Data

dbSNP Id: rs1468031835
gnomAD v2: 5-92920996-C-T
gnomAD v4: 5-93585290-C-T
MyVariant Identifiers: chr5:g.92920996C>T (hg19) chr5:g.93585290C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585290C>T , CM000667.2:g.93585290C>T GRCh38
NC_000005.9:g.92920996C>T , CM000667.1:g.92920996C>T GRCh37
NC_000005.8:g.92946752C>T NCBI36
NG_034119.1:g.6954C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.192C>T ENSP00000481517.1:p.Cys64=
ENST00000327111.8:c.267C>T MANE Select ENSP00000325819.3:p.Cys89=
ENST00000647447.1:c.114C>T ENSP00000495740.1:p.Cys38=
ENST00000327111.7:c.267C>T ENSP00000325819.3:p.Cys89=
ENST00000615873.1:c.192C>T ENSP00000481517.1:p.Cys64=
NM_005654.5:c.267C>T NP_005645.1:p.Cys89=
NM_005654.6:c.267C>T MANE Select NP_005645.1:p.Cys89=
Search 100 bp 5'
Search 100 bp 3'