Canonical Allele Identifier: CA360525882
Gene: NR2F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.92920995G>C (hg19) chr5:g.93585289G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585289G>C , CM000667.2:g.93585289G>C GRCh38
NC_000005.9:g.92920995G>C , CM000667.1:g.92920995G>C GRCh37
NC_000005.8:g.92946751G>C NCBI36
NG_034119.1:g.6953G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.191G>C ENSP00000481517.1:p.Cys64Ser
ENST00000327111.8:c.266G>C MANE Select ENSP00000325819.3:p.Cys89Ser
ENST00000647447.1:c.113G>C ENSP00000495740.1:p.Cys38Ser
ENST00000327111.7:c.266G>C ENSP00000325819.3:p.Cys89Ser
ENST00000615873.1:c.191G>C ENSP00000481517.1:p.Cys64Ser
NM_005654.5:c.266G>C NP_005645.1:p.Cys89Ser
NM_005654.6:c.266G>C MANE Select NP_005645.1:p.Cys89Ser
Search 100 bp 5'
Search 100 bp 3'