Canonical Allele Identifier: CA15618753
Gene: RORB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.74534921A>G , CM000671.2:g.74534921A>G GRCh38
NC_000009.11:g.77149837A>G , CM000671.1:g.77149837A>G GRCh37
NC_000009.10:g.76339657A>G NCBI36
NG_046926.2:g.42586A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376896.8:c.7+36938A>G MANE Select ENSP00000366093.2:n.7+36938A>G
ENST00000376896.7:c.7+36938A>G ENSP00000366093.2:n.7+36938A>G
NM_006914.3:c.7+36938A>G NP_008845.2:n.7+36938A>G
NM_006914.4:c.7+36938A>G MANE Select NP_008845.2:n.7+36938A>G