Canonical Allele Identifier: CA1373067638

Gene: FRMD4B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69203748C= , CM000665.2:g.69203748C=	GRCh38
NC_000003.11:g.69252899C= , CM000665.1:g.69252899C=	GRCh37
NC_000003.10:g.69335589C=	NCBI36
NG_034059.1:g.187557G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398540.8:c.877-4974G= MANE Select	ENSP00000381549.3:n.877-4974G=
ENST00000398540.7:c.877-4974G=	ENSP00000381549.3:n.877-4974G=
ENST00000470070.6:n.771-4974G=
ENST00000483668.5:n.489-4974G=
ENST00000487751.1:n.502-4974G=
NM_015123.2:c.877-4974G=	NP_055938.1:n.877-4974G=
XM_005264721.2:c.910-4974G=	XP_005264778.2:n.910-4974G=
XM_005264722.1:c.742-4974G=	XP_005264779.1:n.742-4974G=
XM_006713063.2:c.715-4974G=	XP_006713126.1:n.715-4974G=
XM_011533526.1:c.715-4974G=	XP_011531828.1:n.715-4974G=
XM_011533527.1:c.142-4974G=	XP_011531829.1:n.142-4974G=
XM_017005989.1:c.877-4974G=	XP_016861478.1:n.877-4974G=
XM_017005990.1:c.742-4974G=	XP_016861479.1:n.742-4974G=
XM_017005991.1:c.715-4974G=	XP_016861480.1:n.715-4974G=
XM_017005992.1:c.715-4974G=	XP_016861481.1:n.715-4974G=
XM_017005993.1:c.715-4974G=	XP_016861482.1:n.715-4974G=
XM_017005994.1:c.715-4974G=	XP_016861483.1:n.715-4974G=
XM_017005995.1:c.142-4974G=	XP_016861484.1:n.142-4974G=
NM_015123.3:c.877-4974G= MANE Select	NP_055938.2:n.877-4974G=