Canonical Allele Identifier: CA889868796

Gene: FCRL3

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.157699878G>C , CM000663.2:g.157699878G>C	GRCh38
NC_000001.10:g.157669668G>C , CM000663.1:g.157669668G>C	GRCh37
NC_000001.9:g.155936292G>C	NCBI36
NG_023241.1:g.5980C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368184.8:c.32-166C>G MANE Select	ENSP00000357167.3:n.32-166C>G
ENST00000368184.7:c.32-166C>G	ENSP00000357167.3:n.32-166C>G
ENST00000368186.9:c.32-166C>G	ENSP00000357169.5:n.32-166C>G
ENST00000477837.5:c.32-166C>G	ENSP00000433430.1:n.32-166C>G
ENST00000480682.5:n.197-166C>G
ENST00000485028.5:c.32-166C>G	ENSP00000434331.1:n.32-166C>G
ENST00000492769.5:c.32-166C>G	ENSP00000435487.1:n.32-166C>G
ENST00000494724.5:n.197-166C>G
ENST00000496769.1:c.32-166C>G	ENSP00000473680.1:n.32-166C>G
NM_052939.3:c.32-166C>G	NP_443171.2:n.32-166C>G
XM_006711145.1:c.32-166C>G	XP_006711208.1:n.32-166C>G
XM_011509138.1:c.32-166C>G	XP_011507440.1:n.32-166C>G
XR_241065.1:n.230-166C>G
NM_001320333.1:c.32-166C>G	NP_001307262.1:n.32-166C>G
NR_135214.1:n.339-166C>G
NR_135215.1:n.339-166C>G
NR_135216.1:n.339-166C>G
NR_135217.1:n.339-166C>G
NM_052939.4:c.32-166C>G MANE Select	NP_443171.2:n.32-166C>G
NM_001320333.2:c.32-166C>G	NP_001307262.1:n.32-166C>G
NR_135214.2:n.236-166C>G
NR_135215.2:n.236-166C>G
NR_135216.2:n.236-166C>G
NR_135217.2:n.236-166C>G