Canonical Allele Identifier: CA1040556345

Gene: MYO1B

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191253321T>A , CM000664.2:g.191253321T>A	GRCh38
NC_000002.11:g.192118047T>A , CM000664.1:g.192118047T>A	GRCh37
NC_000002.10:g.191826292T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392318.8:c.-10+7695T>A MANE Select	ENSP00000376132.3:n.-10+7695T>A
ENST00000304164.8:c.-10+7710T>A	ENSP00000306382.4:n.-10+7710T>A
ENST00000339514.8:c.-10+7695T>A	ENSP00000341903.4:n.-10+7695T>A
ENST00000392318.7:c.-10+7695T>A	ENSP00000376132.3:n.-10+7695T>A
ENST00000418908.5:c.-10+8064T>A	ENSP00000401324.1:n.-10+8064T>A
ENST00000438652.5:c.-10+6954T>A	ENSP00000399459.1:n.-10+6954T>A
NM_001130158.1:c.-10+7695T>A	NP_001123630.1:n.-10+7695T>A
NM_001161819.1:c.-10+7710T>A	NP_001155291.1:n.-10+7710T>A
NM_012223.3:c.-10+7695T>A	NP_036355.2:n.-10+7695T>A
XM_006712536.1:c.-10+6954T>A	XP_006712599.1:n.-10+6954T>A
XM_011511213.1:c.-10+8064T>A	XP_011509515.1:n.-10+8064T>A
NM_001130158.2:c.-10+7695T>A	NP_001123630.1:n.-10+7695T>A
NM_001161819.2:c.-10+7710T>A	NP_001155291.1:n.-10+7710T>A
NM_001330237.1:c.-10+7695T>A	NP_001317166.1:n.-10+7695T>A
NM_001330238.1:c.-10+7695T>A	NP_001317167.1:n.-10+7695T>A
NM_012223.4:c.-10+7695T>A	NP_036355.2:n.-10+7695T>A
XM_024452914.1:c.51+5313T>A	XP_024308682.1:n.51+5313T>A
XM_024452915.1:c.51+5313T>A	XP_024308683.1:n.51+5313T>A
NM_001130158.3:c.-10+7695T>A MANE Select	NP_001123630.1:n.-10+7695T>A
NM_001161819.3:c.-10+7710T>A	NP_001155291.1:n.-10+7710T>A
NM_001330237.2:c.-10+7695T>A	NP_001317166.1:n.-10+7695T>A
NM_001330238.2:c.-10+7695T>A	NP_001317167.1:n.-10+7695T>A
NM_012223.5:c.-10+7695T>A	NP_036355.2:n.-10+7695T>A