Canonical Allele Identifier: CA771906271
Gene: RARA HGNC NCBI

Linked Data

dbSNP Id: rs1368725325
gnomAD v3: 17-40313663-C-T
gnomAD v4: 17-40313663-C-T
MyVariant Identifiers: chr17:g.38469915C>T (hg19) chr17:g.40313663C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40313663C>T , CM000679.2:g.40313663C>T GRCh38
NC_000017.10:g.38469915C>T , CM000679.1:g.38469915C>T GRCh37
NC_000017.9:g.35723441C>T NCBI36
NG_027701.1:g.9493C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000254066.10:c.-363+4377C>T MANE Select ENSP00000254066.5:n.-363+4377C>T
ENST00000254066.9:c.-363+4377C>T ENSP00000254066.5:n.-363+4377C>T
ENST00000577646.5:c.-440+4377C>T ENSP00000464287.1:n.-440+4377C>T
NM_000964.3:c.-363+4377C>T NP_000955.1:n.-363+4377C>T
XM_011525095.1:c.-440+4377C>T XP_011523397.1:n.-440+4377C>T
NM_000964.4:c.-363+4377C>T MANE Select NP_000955.1:n.-363+4377C>T
Search 100 bp 5'
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