Canonical Allele Identifier: CA2259497453

Gene: RARA

Linked Data

• dbSNP Id: rs2033136464

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40313608T>G , CM000679.2:g.40313608T>G	GRCh38
NC_000017.10:g.38469860T>G , CM000679.1:g.38469860T>G	GRCh37
NC_000017.9:g.35723386T>G	NCBI36
NG_027701.1:g.9438T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000254066.10:c.-363+4322T>G MANE Select	ENSP00000254066.5:n.-363+4322T>G
ENST00000254066.9:c.-363+4322T>G	ENSP00000254066.5:n.-363+4322T>G
ENST00000577646.5:c.-440+4322T>G	ENSP00000464287.1:n.-440+4322T>G
NM_000964.3:c.-363+4322T>G	NP_000955.1:n.-363+4322T>G
XM_011525095.1:c.-440+4322T>G	XP_011523397.1:n.-440+4322T>G
NM_000964.4:c.-363+4322T>G MANE Select	NP_000955.1:n.-363+4322T>G