Canonical Allele Identifier: CA1174047

Gene: FCRL5

Linked Data

• dbSNP Id: rs6427384
• ExAC: 1:157508882 C / T
• gnomAD v2: 1-157508882-C-T
• gnomAD v3: 1-157539092-C-T
• gnomAD v4: 1-157539092-C-T
• MyVariant Identifiers: chr1:g.157508882C>T (hg19) ; chr1:g.157539092C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.157539092C>T , CM000663.2:g.157539092C>T	GRCh38
NC_000001.10:g.157508882C>T , CM000663.1:g.157508882C>T	GRCh37
NC_000001.9:g.155775506C>T	NCBI36
NG_027723.1:g.18429G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361835.8:c.1396G>A MANE Select	ENSP00000354691.3:p.Val466Ile
ENST00000361835.7:c.1396G>A	ENSP00000354691.3:p.Val466Ile
ENST00000368189.3:c.1396G>A	ENSP00000357172.3:p.Val466Ile
ENST00000368190.7:c.1396G>A	ENSP00000357173.3:p.Val466Ile
NM_001195388.1:c.1396G>A	NP_001182317.1:p.Val466Ile
NM_031281.2:c.1396G>A	NP_112571.2:p.Val466Ile
XM_011510030.1:c.1141G>A	XP_011508332.1:p.Val381Ile
XM_011510031.1:c.1396G>A	XP_011508333.1:p.Val466Ile
XM_011510032.1:c.1117G>A	XP_011508334.1:p.Val373Ile
XM_011510033.1:c.1396G>A	XP_011508335.1:p.Val466Ile
XM_011510030.2:c.1141G>A	XP_011508332.1:p.Val381Ile
XM_011510031.2:c.1396G>A	XP_011508333.1:p.Val466Ile
XM_011510032.2:c.1117G>A	XP_011508334.1:p.Val373Ile
XM_011510033.2:c.1396G>A	XP_011508335.1:p.Val466Ile
NM_031281.3:c.1396G>A MANE Select	NP_112571.2:p.Val466Ile
NM_001195388.2:c.1396G>A	NP_001182317.1:p.Val466Ile