Canonical Allele Identifier: CA344790126
Gene: FLVCR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 427182
ClinVar RCV Id: RCV000489041
dbSNP Id: rs1085308007
MyVariant Identifiers: chr1:g.213037166G>A (hg19) chr1:g.212863824G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212863824G>A , CM000663.2:g.212863824G>A GRCh38
NC_000001.10:g.213037166G>A , CM000663.1:g.213037166G>A GRCh37
NC_000001.9:g.211103789G>A NCBI36
NG_028131.1:g.10570G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000366971.9:c.838G>A MANE Select ENSP00000355938.4:p.Gly280Arg
ENST00000366971.8:c.838G>A ENSP00000355938.4:p.Gly280Arg
ENST00000419102.1:c.375G>A
ENST00000579295.1:n.194G>A
NM_014053.3:c.838G>A NP_054772.1:p.Gly280Arg
XM_011509446.1:c.838G>A XP_011507748.1:p.Gly280Arg
XM_011509447.1:c.838G>A XP_011507749.1:p.Gly280Arg
XM_011509448.1:c.838G>A XP_011507750.1:p.Gly280Arg
XR_247024.1:n.1012G>A
XR_426771.1:n.1012G>A
XR_426772.2:n.1012G>A
XR_921769.1:n.1012G>A
XM_011509446.3:c.838G>A XP_011507748.1:p.Gly280Arg
XM_011509447.2:c.838G>A XP_011507749.1:p.Gly280Arg
XR_247024.3:n.1012G>A
XR_426772.3:n.1012G>A
NM_014053.4:c.838G>A MANE Select NP_054772.1:p.Gly280Arg
Search 100 bp 5'
Search 100 bp 3'