Canonical Allele Identifier: CA8768665

Gene: ITGB4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75727859C>T , CM000679.2:g.75727859C>T	GRCh38
NC_000017.10:g.73723940C>T , CM000679.1:g.73723940C>T	GRCh37
NC_000017.9:g.71235535C>T	NCBI36
NG_007372.1:g.11425C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449880.7:c.469+4C>T	ENSP00000400217.2:n.469+4C>T
ENST00000200181.8:c.469+4C>T MANE Select	ENSP00000200181.3:n.469+4C>T
ENST00000200181.7:c.469+4C>T	ENSP00000200181.3:n.469+4C>T
ENST00000449880.6:c.469+4C>T	ENSP00000400217.2:n.469+4C>T
ENST00000450894.7:c.469+4C>T	ENSP00000405536.3:n.469+4C>T
ENST00000579662.5:c.469+4C>T	ENSP00000463651.1:n.469+4C>T
ENST00000580542.5:n.534+4C>T
ENST00000582629.1:c.55+4C>T	ENSP00000463788.1:n.55+4C>T
ENST00000584558.5:n.469+4C>T
NM_000213.3:c.469+4C>T	NP_000204.3:n.469+4C>T
NM_001005619.1:c.469+4C>T	NP_001005619.1:n.469+4C>T
NM_001005731.1:c.469+4C>T	NP_001005731.1:n.469+4C>T
XM_005257309.2:c.469+4C>T	XP_005257366.1:n.469+4C>T
XM_005257311.3:c.469+4C>T	XP_005257368.1:n.469+4C>T
XM_005257312.2:c.469+4C>T	XP_005257369.1:n.469+4C>T
XM_006721866.2:c.574+4C>T	XP_006721929.1:n.574+4C>T
XM_006721867.2:c.574+4C>T	XP_006721930.1:n.574+4C>T
XM_006721868.2:c.574+4C>T	XP_006721931.1:n.574+4C>T
XM_006721870.2:c.574+4C>T	XP_006721933.1:n.574+4C>T
XM_011524751.1:c.574+4C>T	XP_011523053.1:n.574+4C>T
NM_000213.4:c.469+4C>T	NP_000204.3:n.469+4C>T
NM_001005731.2:c.469+4C>T	NP_001005731.1:n.469+4C>T
NM_001321123.1:c.469+4C>T	NP_001308052.1:n.469+4C>T
XM_005257311.4:c.469+4C>T	XP_005257368.1:n.469+4C>T
XM_006721866.3:c.574+4C>T	XP_006721929.1:n.574+4C>T
XM_006721867.3:c.574+4C>T	XP_006721930.1:n.574+4C>T
XM_006721868.3:c.574+4C>T	XP_006721931.1:n.574+4C>T
XM_006721870.3:c.574+4C>T	XP_006721933.1:n.574+4C>T
XM_011524751.2:c.574+4C>T	XP_011523053.1:n.574+4C>T
NM_000213.5:c.469+4C>T MANE Select	NP_000204.3:n.469+4C>T
NM_001005731.3:c.469+4C>T	NP_001005731.1:n.469+4C>T
NM_001321123.2:c.469+4C>T	NP_001308052.1:n.469+4C>T