Canonical Allele Identifier: CA423300474
Gene: FLVCR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.213056738A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883396A>G , CM000663.2:g.212883396A>G GRCh38
NC_000001.10:g.213056738A>G , CM000663.1:g.213056738A>G GRCh37
NC_000001.9:g.211123361A>G NCBI36
NG_028131.1:g.30142A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1050A>G MANE Select ENSP00000355938.4:p.Ser350=
ENST00000366971.8:c.1050A>G ENSP00000355938.4:p.Ser350=
ENST00000419102.1:c.446A>G
ENST00000474693.1:n.275A>G
NM_014053.3:c.1050A>G NP_054772.1:p.Ser350=
XM_011509446.1:c.1050A>G XP_011507748.1:p.Ser350=
XR_247024.1:n.1224A>G
XR_426771.1:n.1351A>G
XM_011509446.3:c.1050A>G XP_011507748.1:p.Ser350=
XR_247024.3:n.1224A>G
NM_014053.4:c.1050A>G MANE Select NP_054772.1:p.Ser350=