Canonical Allele Identifier: CA360525901
Gene: NR2F1 HGNC NCBI

Linked Data

dbSNP Id: rs1753210791
MyVariant Identifiers: chr5:g.92921003A>C (hg19) chr5:g.93585297A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585297A>C , CM000667.2:g.93585297A>C GRCh38
NC_000005.9:g.92921003A>C , CM000667.1:g.92921003A>C GRCh37
NC_000005.8:g.92946759A>C NCBI36
NG_034119.1:g.6961A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.199A>C ENSP00000481517.1:p.Lys67Gln
ENST00000327111.8:c.274A>C MANE Select ENSP00000325819.3:p.Lys92Gln
ENST00000647447.1:c.121A>C ENSP00000495740.1:p.Lys41Gln
ENST00000327111.7:c.274A>C ENSP00000325819.3:p.Lys92Gln
ENST00000615873.1:c.199A>C ENSP00000481517.1:p.Lys67Gln
NM_005654.5:c.274A>C NP_005645.1:p.Lys92Gln
NM_005654.6:c.274A>C MANE Select NP_005645.1:p.Lys92Gln
Search 100 bp 5'
Search 100 bp 3'