Canonical Allele Identifier: CA889868695

Gene: FCRL3

Linked Data

• dbSNP Id: rs3761959
• gnomAD v3: 1-157699488-C-G
• gnomAD v4: 1-157699488-C-G
• MyVariant Identifiers: chr1:g.157669278C>G (hg19) ; chr1:g.157699488C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.157699488C>G , CM000663.2:g.157699488C>G	GRCh38
NC_000001.10:g.157669278C>G , CM000663.1:g.157669278C>G	GRCh37
NC_000001.9:g.155935902C>G	NCBI36
NG_023241.1:g.6370G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368184.8:c.52+204G>C MANE Select	ENSP00000357167.3:n.52+204G>C
ENST00000368184.7:c.52+204G>C	ENSP00000357167.3:n.52+204G>C
ENST00000368186.9:c.52+204G>C	ENSP00000357169.5:n.52+204G>C
ENST00000477837.5:c.52+204G>C	ENSP00000433430.1:n.52+204G>C
ENST00000480682.5:n.217+204G>C
ENST00000485028.5:c.52+204G>C	ENSP00000434331.1:n.52+204G>C
ENST00000492769.5:c.52+204G>C	ENSP00000435487.1:n.52+204G>C
ENST00000494724.5:n.217+204G>C
ENST00000496769.1:c.52+204G>C	ENSP00000473680.1:n.52+204G>C
NM_052939.3:c.52+204G>C	NP_443171.2:n.52+204G>C
XM_006711145.1:c.52+204G>C	XP_006711208.1:n.52+204G>C
XM_011509138.1:c.52+204G>C	XP_011507440.1:n.52+204G>C
XR_241065.1:n.250+204G>C
NM_001320333.1:c.52+204G>C	NP_001307262.1:n.52+204G>C
NR_135214.1:n.359+204G>C
NR_135215.1:n.359+204G>C
NR_135216.1:n.359+204G>C
NR_135217.1:n.359+204G>C
NM_052939.4:c.52+204G>C MANE Select	NP_443171.2:n.52+204G>C
NM_001320333.2:c.52+204G>C	NP_001307262.1:n.52+204G>C
NR_135214.2:n.256+204G>C
NR_135215.2:n.256+204G>C
NR_135216.2:n.256+204G>C
NR_135217.2:n.256+204G>C