Canonical Allele Identifier: CA731118636
Gene: FLVCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1241680178
MyVariant Identifiers: chr1:g.213056482T>G (hg19) chr1:g.212883140T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.212883140T>G , CM000663.2:g.212883140T>G GRCh38
NC_000001.10:g.213056482T>G , CM000663.1:g.213056482T>G GRCh37
NC_000001.9:g.211123105T>G NCBI36
NG_028131.1:g.29886T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000366971.9:c.1025-231T>G MANE Select ENSP00000355938.4:n.1025-231T>G
ENST00000366971.8:c.1025-231T>G ENSP00000355938.4:n.1025-231T>G
ENST00000419102.1:c.421-231T>G
ENST00000474693.1:n.250-231T>G
NM_014053.3:c.1025-231T>G NP_054772.1:n.1025-231T>G
XM_011509446.1:c.1025-231T>G XP_011507748.1:n.1025-231T>G
XR_247024.1:n.1199-231T>G
XR_426771.1:n.1326-231T>G
XM_011509446.3:c.1025-231T>G XP_011507748.1:n.1025-231T>G
XR_247024.3:n.1199-231T>G
NM_014053.4:c.1025-231T>G MANE Select NP_054772.1:n.1025-231T>G
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