Canonical Allele Identifier: CA393929942
Gene: NR2F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.96875589G>T (hg19) chr15:g.96332360G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96332360G>T , CM000677.2:g.96332360G>T GRCh38
NC_000015.9:g.96875589G>T , CM000677.1:g.96875589G>T GRCh37
NC_000015.8:g.94676593G>T NCBI36
NG_016753.1:g.11433G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000394166.8:c.255G>T MANE Select ENSP00000377721.3:p.Lys85Asn
ENST00000394166.7:c.255G>T ENSP00000377721.3:p.Lys85Asn
ENST00000421109.6:c.44-1716G>T ENSP00000401674.2:n.44-1716G>T
NM_001145155.1:c.44-1716G>T NP_001138627.1:n.44-1716G>T
NM_021005.3:c.255G>T NP_066285.1:p.Lys85Asn
NM_021005.4:c.255G>T MANE Select NP_066285.1:p.Lys85Asn
NM_001145155.2:c.44-1716G>T NP_001138627.1:n.44-1716G>T
Search 100 bp 5'
Search 100 bp 3'