Canonical Allele Identifier: CA290504457
Gene: RARA HGNC NCBI

Linked Data

dbSNP Id: rs974452291
MyVariant Identifiers: chr17:g.38470104G>A (hg19) chr17:g.40313852G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40313852G>A , CM000679.2:g.40313852G>A GRCh38
NC_000017.10:g.38470104G>A , CM000679.1:g.38470104G>A GRCh37
NC_000017.9:g.35723630G>A NCBI36
NG_027701.1:g.9682G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000254066.10:c.-363+4566G>A MANE Select ENSP00000254066.5:n.-363+4566G>A
ENST00000254066.9:c.-363+4566G>A ENSP00000254066.5:n.-363+4566G>A
ENST00000577646.5:c.-440+4566G>A ENSP00000464287.1:n.-440+4566G>A
NM_000964.3:c.-363+4566G>A NP_000955.1:n.-363+4566G>A
XM_011525095.1:c.-440+4566G>A XP_011523397.1:n.-440+4566G>A
NM_000964.4:c.-363+4566G>A MANE Select NP_000955.1:n.-363+4566G>A
Search 100 bp 5'
Search 100 bp 3'