Canonical Allele Identifier: CA2485643330
Gene: FLVCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1664968769

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883220T>C , CM000663.2:g.212883220T>C GRCh38
NC_000001.10:g.213056562T>C , CM000663.1:g.213056562T>C GRCh37
NC_000001.9:g.211123185T>C NCBI36
NG_028131.1:g.29966T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1025-151T>C MANE Select ENSP00000355938.4:n.1025-151T>C
ENST00000366971.8:c.1025-151T>C ENSP00000355938.4:n.1025-151T>C
ENST00000419102.1:c.421-151T>C
ENST00000474693.1:n.250-151T>C
NM_014053.3:c.1025-151T>C NP_054772.1:n.1025-151T>C
XM_011509446.1:c.1025-151T>C XP_011507748.1:n.1025-151T>C
XR_247024.1:n.1199-151T>C
XR_426771.1:n.1326-151T>C
XM_011509446.3:c.1025-151T>C XP_011507748.1:n.1025-151T>C
XR_247024.3:n.1199-151T>C
NM_014053.4:c.1025-151T>C MANE Select NP_054772.1:n.1025-151T>C