Canonical Allele Identifier: CA10640511

Gene: ITGB4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75721498G>C , CM000679.2:g.75721498G>C	GRCh38
NC_000017.10:g.73717578G>C , CM000679.1:g.73717578G>C	GRCh37
NC_000017.9:g.71229173G>C	NCBI36
NG_007372.1:g.5063G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000213.5:c.-125G>C MANE Select	NP_000204.3:n.-125G>C
ENST00000200181.8:c.-125G>C MANE Select	ENSP00000200181.3:n.-125G>C
NM_000213.3:c.-125G>C	NP_000204.3:n.-125G>C
NM_000213.4:c.-125G>C	NP_000204.3:n.-125G>C
NM_001005731.1:c.-125G>C	NP_001005731.1:n.-125G>C
NM_001005731.2:c.-125G>C	NP_001005731.1:n.-125G>C
NM_001005731.3:c.-125G>C	NP_001005731.1:n.-125G>C
NM_001321123.1:c.-76G>C	NP_001308052.1:n.-76G>C
NM_001321123.2:c.-76G>C	NP_001308052.1:n.-76G>C
ENST00000200181.7:c.-125G>C	ENSP00000200181.3:n.-125G>C
ENST00000449880.7:c.-125G>C	ENSP00000400217.2:n.-125G>C
ENST00000450894.7:c.-125G>C	ENSP00000405536.3:n.-125G>C
ENST00000579662.5:c.-76G>C	ENSP00000463651.1:n.-76G>C
XM_005257311.3:c.-125G>C	XP_005257368.1:n.-125G>C
XM_005257311.4:c.-125G>C	XP_005257368.1:n.-125G>C