Canonical Allele Identifier: CA360525891
Gene: NR2F1 HGNC NCBI

Linked Data

gnomAD v4: 5-93585292-G-C
MyVariant Identifiers: chr5:g.92920998G>C (hg19) chr5:g.93585292G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.93585292G>C , CM000667.2:g.93585292G>C GRCh38
NC_000005.9:g.92920998G>C , CM000667.1:g.92920998G>C GRCh37
NC_000005.8:g.92946754G>C NCBI36
NG_034119.1:g.6956G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000615873.2:c.194G>C ENSP00000481517.1:p.Gly65Ala
ENST00000327111.8:c.269G>C MANE Select ENSP00000325819.3:p.Gly90Ala
ENST00000647447.1:c.116G>C ENSP00000495740.1:p.Gly39Ala
ENST00000327111.7:c.269G>C ENSP00000325819.3:p.Gly90Ala
ENST00000615873.1:c.194G>C ENSP00000481517.1:p.Gly65Ala
NM_005654.5:c.269G>C NP_005645.1:p.Gly90Ala
NM_005654.6:c.269G>C MANE Select NP_005645.1:p.Gly90Ala
Search 100 bp 5'
Search 100 bp 3'