Canonical Allele Identifier: CA771906248
Gene: RARA HGNC NCBI

Linked Data

dbSNP Id: rs1203776093
MyVariant Identifiers: chr17:g.38469853T>C (hg19) chr17:g.40313601T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40313601T>C , CM000679.2:g.40313601T>C GRCh38
NC_000017.10:g.38469853T>C , CM000679.1:g.38469853T>C GRCh37
NC_000017.9:g.35723379T>C NCBI36
NG_027701.1:g.9431T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000254066.10:c.-363+4315T>C MANE Select ENSP00000254066.5:n.-363+4315T>C
ENST00000254066.9:c.-363+4315T>C ENSP00000254066.5:n.-363+4315T>C
ENST00000577646.5:c.-440+4315T>C ENSP00000464287.1:n.-440+4315T>C
NM_000964.3:c.-363+4315T>C NP_000955.1:n.-363+4315T>C
XM_011525095.1:c.-440+4315T>C XP_011523397.1:n.-440+4315T>C
NM_000964.4:c.-363+4315T>C MANE Select NP_000955.1:n.-363+4315T>C
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