Canonical Allele Identifier: CA731118638

Gene: FLVCR1

Linked Data

• dbSNP Id: rs1235340530
• gnomAD v3: 1-212883152-A-G
• gnomAD v4: 1-212883152-A-G
• MyVariant Identifiers: chr1:g.213056494A>G (hg19) ; chr1:g.212883152A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.212883152A>G , CM000663.2:g.212883152A>G	GRCh38
NC_000001.10:g.213056494A>G , CM000663.1:g.213056494A>G	GRCh37
NC_000001.9:g.211123117A>G	NCBI36
NG_028131.1:g.29898A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366971.9:c.1025-219A>G MANE Select	ENSP00000355938.4:n.1025-219A>G
ENST00000366971.8:c.1025-219A>G	ENSP00000355938.4:n.1025-219A>G
ENST00000419102.1:c.421-219A>G
ENST00000474693.1:n.250-219A>G
NM_014053.3:c.1025-219A>G	NP_054772.1:n.1025-219A>G
XM_011509446.1:c.1025-219A>G	XP_011507748.1:n.1025-219A>G
XR_247024.1:n.1199-219A>G
XR_426771.1:n.1326-219A>G
XM_011509446.3:c.1025-219A>G	XP_011507748.1:n.1025-219A>G
XR_247024.3:n.1199-219A>G
NM_014053.4:c.1025-219A>G MANE Select	NP_054772.1:n.1025-219A>G