Canonical Allele Identifier: CA2259497580
Gene: RARA HGNC NCBI

Linked Data

dbSNP Id: rs2033141988

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40313889A>C , CM000679.2:g.40313889A>C GRCh38
NC_000017.10:g.38470141A>C , CM000679.1:g.38470141A>C GRCh37
NC_000017.9:g.35723667A>C NCBI36
NG_027701.1:g.9719A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000254066.10:c.-363+4603A>C MANE Select ENSP00000254066.5:n.-363+4603A>C
ENST00000254066.9:c.-363+4603A>C ENSP00000254066.5:n.-363+4603A>C
ENST00000577646.5:c.-440+4603A>C ENSP00000464287.1:n.-440+4603A>C
NM_000964.3:c.-363+4603A>C NP_000955.1:n.-363+4603A>C
XM_011525095.1:c.-440+4603A>C XP_011523397.1:n.-440+4603A>C
NM_000964.4:c.-363+4603A>C MANE Select NP_000955.1:n.-363+4603A>C