Canonical Allele Identifier: CA1012017898
Gene: FLVCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1664966337

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883077A>G , CM000663.2:g.212883077A>G GRCh38
NC_000001.10:g.213056419A>G , CM000663.1:g.213056419A>G GRCh37
NC_000001.9:g.211123042A>G NCBI36
NG_028131.1:g.29823A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1025-294A>G MANE Select ENSP00000355938.4:n.1025-294A>G
ENST00000366971.8:c.1025-294A>G ENSP00000355938.4:n.1025-294A>G
ENST00000419102.1:c.421-294A>G
ENST00000474693.1:n.250-294A>G
NM_014053.3:c.1025-294A>G NP_054772.1:n.1025-294A>G
XM_011509446.1:c.1025-294A>G XP_011507748.1:n.1025-294A>G
XR_247024.1:n.1199-294A>G
XR_426771.1:n.1326-294A>G
XM_011509446.3:c.1025-294A>G XP_011507748.1:n.1025-294A>G
XR_247024.3:n.1199-294A>G
NM_014053.4:c.1025-294A>G MANE Select NP_054772.1:n.1025-294A>G