Canonical Allele Identifier: CA423300493
Gene: FLVCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.213056771A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883429A>G , CM000663.2:g.212883429A>G GRCh38
NC_000001.10:g.213056771A>G , CM000663.1:g.213056771A>G GRCh37
NC_000001.9:g.211123394A>G NCBI36
NG_028131.1:g.30175A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1083A>G MANE Select ENSP00000355938.4:p.Thr361=
ENST00000366971.8:c.1083A>G ENSP00000355938.4:p.Thr361=
ENST00000419102.1:c.479A>G
ENST00000474693.1:n.308A>G
ENST00000483790.1:n.21A>G
NM_014053.3:c.1083A>G NP_054772.1:p.Thr361=
XM_011509446.1:c.1083A>G XP_011507748.1:p.Thr361=
XR_247024.1:n.1257A>G
XR_426771.1:n.1384A>G
XM_011509446.3:c.1083A>G XP_011507748.1:p.Thr361=
XR_247024.3:n.1257A>G
NM_014053.4:c.1083A>G MANE Select NP_054772.1:p.Thr361=