Canonical Allele Identifier: CA492689926
Gene: NR2F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.96877807C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.96334578C>G , CM000677.2:g.96334578C>G GRCh38
NC_000015.9:g.96877807C>G , CM000677.1:g.96877807C>G GRCh37
NC_000015.8:g.94678811C>G NCBI36
NG_016753.1:g.13651C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394166.8:c.945C>G MANE Select ENSP00000377721.3:p.Leu315=
ENST00000394166.7:c.945C>G ENSP00000377721.3:p.Leu315=
ENST00000394171.6:c.486C>G ENSP00000377726.2:p.Leu162=
ENST00000421109.6:c.546C>G ENSP00000401674.2:p.Leu182=
ENST00000453270.2:c.486C>G ENSP00000389853.2:p.Leu162=
NM_001145155.1:c.546C>G NP_001138627.1:p.Leu182=
NM_001145156.1:c.486C>G NP_001138628.1:p.Leu162=
NM_001145157.1:c.486C>G NP_001138629.1:p.Leu162=
NM_021005.3:c.945C>G NP_066285.1:p.Leu315=
NM_021005.4:c.945C>G MANE Select NP_066285.1:p.Leu315=
NM_001145155.2:c.546C>G NP_001138627.1:p.Leu182=
NM_001145157.2:c.486C>G NP_001138629.1:p.Leu162=