Canonical Allele Identifier: CA351961997

Gene: LRRC3B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.26710330T>C , CM000665.2:g.26710330T>C	GRCh38
NC_000003.11:g.26751821T>C , CM000665.1:g.26751821T>C	GRCh37
NC_000003.10:g.26726825T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396641.7:c.658T>C MANE Select	ENSP00000379880.2:p.Tyr220His
ENST00000648296.1:c.658T>C	ENSP00000497471.1:p.Tyr220His
ENST00000396641.6:c.658T>C	ENSP00000379880.2:p.Tyr220His
ENST00000417744.5:c.658T>C	ENSP00000406370.1:p.Tyr220His
ENST00000456208.2:c.658T>C	ENSP00000394940.2:p.Tyr220His
NM_052953.2:c.658T>C	NP_443185.1:p.Tyr220His
XM_005264847.2:c.658T>C	XP_005264904.1:p.Tyr220His
XM_005264849.2:c.658T>C	XP_005264906.1:p.Tyr220His
XM_005264850.3:c.658T>C	XP_005264907.1:p.Tyr220His
XM_011533332.1:c.658T>C	XP_011531634.1:p.Tyr220His
XM_011533333.1:c.658T>C	XP_011531635.1:p.Tyr220His
NM_001317808.1:c.658T>C	NP_001304737.1:p.Tyr220His
NM_001317809.1:c.658T>C	NP_001304738.1:p.Tyr220His
NM_001317810.1:c.658T>C	NP_001304739.1:p.Tyr220His
NM_001317811.1:c.658T>C	NP_001304740.1:p.Tyr220His
NM_052953.3:c.658T>C	NP_443185.1:p.Tyr220His
XM_005264849.3:c.658T>C	XP_005264906.1:p.Tyr220His
XM_005264850.4:c.658T>C	XP_005264907.1:p.Tyr220His
XM_011533332.3:c.658T>C	XP_011531634.1:p.Tyr220His
XM_017005675.1:c.658T>C	XP_016861164.1:p.Tyr220His
XR_001739997.1:n.2293T>C
XR_001739998.1:n.2293T>C
XR_001739999.1:n.2293T>C
NM_001317808.2:c.658T>C	NP_001304737.1:p.Tyr220His
NM_001317809.2:c.658T>C	NP_001304738.1:p.Tyr220His
NM_001317810.2:c.658T>C	NP_001304739.1:p.Tyr220His
NM_001317811.2:c.658T>C	NP_001304740.1:p.Tyr220His
NM_052953.4:c.658T>C MANE Select	NP_443185.1:p.Tyr220His
NM_001317810.3:c.658T>C	NP_001304739.1:p.Tyr220His
NM_001395645.1:c.658T>C	NP_001382574.1:p.Tyr220His
NM_001395646.1:c.658T>C	NP_001382575.1:p.Tyr220His
NM_001395647.1:c.658T>C	NP_001382576.1:p.Tyr220His