Canonical Allele Identifier: CA15589366

Gene: MOB3B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27488094T>G , CM000671.2:g.27488094T>G	GRCh38
NC_000009.11:g.27488092T>G , CM000671.1:g.27488092T>G	GRCh37
NC_000009.10:g.27478092T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262244.6:c.-198-32346A>C MANE Select	ENSP00000262244.5:n.-198-32346A>C
ENST00000262244.5:c.-198-32346A>C	ENSP00000262244.5:n.-198-32346A>C
NM_024761.4:c.-198-32346A>C	NP_079037.3:n.-198-32346A>C
NM_024761.5:c.-198-32346A>C MANE Select	NP_079037.3:n.-198-32346A>C