Canonical Allele Identifier: CA360525893
Gene: NR2F1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.92921000G>C (hg19) chr5:g.93585294G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585294G>C , CM000667.2:g.93585294G>C GRCh38
NC_000005.9:g.92921000G>C , CM000667.1:g.92921000G>C GRCh37
NC_000005.8:g.92946756G>C NCBI36
NG_034119.1:g.6958G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.196G>C ENSP00000481517.1:p.Asp66His
ENST00000327111.8:c.271G>C MANE Select ENSP00000325819.3:p.Asp91His
ENST00000647447.1:c.118G>C ENSP00000495740.1:p.Asp40His
ENST00000327111.7:c.271G>C ENSP00000325819.3:p.Asp91His
ENST00000615873.1:c.196G>C ENSP00000481517.1:p.Asp66His
NM_005654.5:c.271G>C NP_005645.1:p.Asp91His
NM_005654.6:c.271G>C MANE Select NP_005645.1:p.Asp91His
Search 100 bp 5'
Search 100 bp 3'