Canonical Allele Identifier: CA2485643422
Gene: FLVCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1664973952

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883459G>C , CM000663.2:g.212883459G>C GRCh38
NC_000001.10:g.213056801G>C , CM000663.1:g.213056801G>C GRCh37
NC_000001.9:g.211123424G>C NCBI36
NG_028131.1:g.30205G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1092+21G>C MANE Select ENSP00000355938.4:n.1092+21G>C
ENST00000366971.8:c.1092+21G>C ENSP00000355938.4:n.1092+21G>C
ENST00000419102.1:c.488+21G>C
ENST00000474693.1:n.317+21G>C
ENST00000483790.1:n.30+21G>C
NM_014053.3:c.1092+21G>C NP_054772.1:n.1092+21G>C
XM_011509446.1:c.1092+21G>C XP_011507748.1:n.1092+21G>C
XR_247024.1:n.1266+21G>C
XR_426771.1:n.1393+21G>C
XM_011509446.3:c.1092+21G>C XP_011507748.1:n.1092+21G>C
XR_247024.3:n.1266+21G>C
NM_014053.4:c.1092+21G>C MANE Select NP_054772.1:n.1092+21G>C