Canonical Allele Identifier: CA11192329

Gene: VWA3B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98244594C>T , CM000664.2:g.98244594C>T	GRCh38
NC_000002.11:g.98861057C>T , CM000664.1:g.98861057C>T	GRCh37
NC_000002.10:g.98227489C>T	NCBI36
NG_054753.1:g.162463C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477737.6:c.2674-5724C>T MANE Select	ENSP00000417955.1:n.2674-5724C>T
ENST00000409460.5:n.2880-5724C>T
ENST00000432242.5:c.*2427-5724C>T	ENSP00000396734.1:n.*2427-5724C>T
ENST00000465555.1:c.140+2296C>T
ENST00000473149.5:c.905-5724C>T
ENST00000477737.5:c.2674-5724C>T	ENSP00000417955.1:n.2674-5724C>T
ENST00000489630.5:c.774-5724C>T
ENST00000495571.5:c.1336-5724C>T
NM_144992.4:c.2674-5724C>T	NP_659429.4:n.2674-5724C>T
XM_005263897.1:c.2674-5724C>T	XP_005263954.1:n.2674-5724C>T
XM_006712357.1:c.2224-5724C>T	XP_006712420.1:n.2224-5724C>T
XM_006712359.2:c.1231-5724C>T	XP_006712422.1:n.1231-5724C>T
XM_006712360.2:c.850-5724C>T	XP_006712423.1:n.850-5724C>T
XM_011510770.1:c.2674-5724C>T	XP_011509072.1:n.2674-5724C>T
XM_011510771.1:c.2548-5724C>T	XP_011509073.1:n.2548-5724C>T
XM_011510772.1:c.2674-5724C>T	XP_011509074.1:n.2674-5724C>T
XM_011510773.1:c.2674-5724C>T	XP_011509075.1:n.2674-5724C>T
XR_244881.1:n.1336-5724C>T
XR_922884.1:n.2903-5724C>T
XR_922885.1:n.2903-5724C>T
XR_922886.1:n.2903-5724C>T
NM_001345864.1:c.1645-5724C>T	NP_001332793.1:n.1645-5724C>T
NR_144296.1:n.2997-5724C>T
XM_005263897.2:c.2674-5724C>T	XP_005263954.1:n.2674-5724C>T
XM_006712357.2:c.2224-5724C>T	XP_006712420.1:n.2224-5724C>T
XM_006712359.3:c.1231-5724C>T	XP_006712422.1:n.1231-5724C>T
XM_011510771.2:c.2548-5724C>T	XP_011509073.1:n.2548-5724C>T
XM_017003561.1:c.1645-5724C>T	XP_016859050.1:n.1645-5724C>T
XM_017003562.1:c.1645-5724C>T	XP_016859051.1:n.1645-5724C>T
XM_017003564.1:c.2674-5724C>T	XP_016859053.1:n.2674-5724C>T
XM_024452744.1:c.1645-5724C>T	XP_024308512.1:n.1645-5724C>T
XR_922885.3:n.2903-5724C>T
NM_001345864.2:c.1645-5724C>T	NP_001332793.1:n.1645-5724C>T
NM_144992.5:c.2674-5724C>T MANE Select	NP_659429.4:n.2674-5724C>T
NR_144296.2:n.2962-5724C>T