Canonical Allele Identifier: CA1657300342

Gene: RWDD1

Linked Data

• dbSNP Id: rs1775170655
• gnomAD v4: 6-116592902-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116592902G>C , CM000668.2:g.116592902G>C	GRCh38
NC_000006.11:g.116914065G>C , CM000668.1:g.116914065G>C	GRCh37
NC_000006.10:g.117020758G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466444.7:c.611-78G>C MANE Select	ENSP00000420357.2:n.611-78G>C
ENST00000466444.6:c.611-78G>C	ENSP00000420357.2:n.611-78G>C
ENST00000487832.6:c.323-78G>C	ENSP00000428778.1:n.323-78G>C
NM_001007464.2:c.323-78G>C	NP_001007465.1:n.323-78G>C
NM_015952.3:c.611-78G>C	NP_057036.2:n.611-78G>C
NM_016104.3:c.323-78G>C	NP_057188.2:n.323-78G>C
NM_015952.4:c.611-78G>C MANE Select	NP_057036.2:n.611-78G>C
NM_001007464.3:c.323-78G>C	NP_001007465.1:n.323-78G>C
NM_016104.4:c.323-78G>C	NP_057188.2:n.323-78G>C