Canonical Allele Identifier: CA1554592717

Gene: MAP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.72114529G= , CM000667.2:g.72114529G=	GRCh38
NC_000005.9:g.71410356G= , CM000667.1:g.71410356G=	GRCh37
NC_000005.8:g.71446112G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296755.12:c.185-1169G= MANE Select	ENSP00000296755.7:n.185-1169G=
ENST00000296755.11:c.185-1169G=	ENSP00000296755.7:n.185-1169G=
ENST00000504183.1:n.240-1169G=
ENST00000511641.2:c.185-1169G=	ENSP00000423444.2:n.185-1169G=
ENST00000512974.5:c.185-1169G=	ENSP00000426312.1:n.185-1169G=
ENST00000513526.6:c.185-1169G=	ENSP00000427194.2:n.185-1169G=
NM_005909.3:c.185-1169G=	NP_005900.2:n.185-1169G=
NM_005909.4:c.185-1169G=	NP_005900.2:n.185-1169G=
NM_005909.5:c.185-1169G= MANE Select	NP_005900.2:n.185-1169G=