Canonical Allele Identifier: CA15406460

Gene: MAP1B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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