Canonical Allele Identifier: CA423300475
Gene: FLVCR1 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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