Canonical Allele Identifier: CA45525670

Gene: RMDN2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38050689T>C , CM000664.2:g.38050689T>C	GRCh38
NC_000002.11:g.38277832T>C , CM000664.1:g.38277832T>C	GRCh37
NC_000002.10:g.38131336T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234195.7:c.1714-16293T>C	ENSP00000234195.3:n.1714-16293T>C
ENST00000469469.1:n.295-16293T>C
NM_144713.4:c.1714-16293T>C	NP_653314.3:n.1714-16293T>C
XM_011532613.1:c.1714-4051T>C	XP_011530915.1:n.1714-4051T>C
XM_011532614.1:c.1714-4051T>C	XP_011530916.1:n.1714-4051T>C
XM_011532616.1:c.1180-4051T>C	XP_011530918.1:n.1180-4051T>C
XM_011532617.1:c.1180-4051T>C	XP_011530919.1:n.1180-4051T>C
XM_011532618.1:c.1180-4051T>C	XP_011530920.1:n.1180-4051T>C
XM_011532619.1:c.1180-4051T>C	XP_011530921.1:n.1180-4051T>C
XM_011532620.1:c.745-4051T>C	XP_011530922.1:n.745-4051T>C
XR_939668.1:n.1982-16293T>C
NM_001322212.1:c.1180-16293T>C	NP_001309141.1:n.1180-16293T>C
XM_011532613.3:c.1714-4051T>C	XP_011530915.1:n.1714-4051T>C
XM_011532614.3:c.1714-4051T>C	XP_011530916.1:n.1714-4051T>C
XM_011532615.3:c.*28-16293T>C	XP_011530917.2:n.*28-16293T>C
XM_011532616.2:c.1180-4051T>C	XP_011530918.1:n.1180-4051T>C
XM_011532617.2:c.1180-4051T>C	XP_011530919.1:n.1180-4051T>C
XM_011532618.2:c.1180-4051T>C	XP_011530920.1:n.1180-4051T>C
XM_011532619.2:c.1180-4051T>C	XP_011530921.1:n.1180-4051T>C
XM_017003475.2:c.1714-16293T>C	XP_016858964.1:n.1714-16293T>C
XM_017003479.1:c.745-4051T>C	XP_016858968.1:n.745-4051T>C
XR_939668.3:n.2113-16293T>C
NM_001322212.2:c.1180-16293T>C	NP_001309141.1:n.1180-16293T>C
NM_144713.5:c.1714-16293T>C	NP_653314.3:n.1714-16293T>C