Canonical Allele Identifier: CA1614487040

Gene: MBOAT1

Linked Data

• dbSNP Id: rs1202199

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.20155943T>G , CM000668.2:g.20155943T>G	GRCh38
NC_000006.11:g.20156174T>G , CM000668.1:g.20156174T>G	GRCh37
NC_000006.10:g.20264153T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000324607.8:c.100-3174A>C MANE Select	ENSP00000324944.7:n.100-3174A>C
ENST00000324607.7:c.100-3174A>C	ENSP00000324944.7:n.100-3174A>C
NM_001080480.2:c.100-3174A>C	NP_001073949.1:n.100-3174A>C
NR_073465.1:n.330-11628A>C
XM_006714999.1:c.4-3174A>C	XP_006715062.1:n.4-3174A>C
XM_006715000.2:c.100-3174A>C	XP_006715063.1:n.100-3174A>C
XM_011514313.1:c.100-3174A>C	XP_011512615.1:n.100-3174A>C
XR_926070.1:n.268-3174A>C
XR_926071.1:n.268-3174A>C
XM_006714999.2:c.4-3174A>C	XP_006715062.1:n.4-3174A>C
XM_006715000.4:c.100-3174A>C	XP_006715063.1:n.100-3174A>C
XM_011514313.3:c.100-3174A>C	XP_011512615.1:n.100-3174A>C
NM_001080480.3:c.100-3174A>C MANE Select	NP_001073949.1:n.100-3174A>C
NR_073465.2:n.335-11628A>C