Canonical Allele Identifier: CA461121139

Gene: CYP7B1

Linked Data

• MyVariant Identifiers: chr8:g.65537069T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64624512T>C , CM000670.2:g.64624512T>C	GRCh38
NC_000008.10:g.65537069T>C , CM000670.1:g.65537069T>C	GRCh37
NC_000008.9:g.65699623T>C	NCBI36
NG_008338.1:g.179280A>G
NG_008338.2:g.179280A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.150A>G MANE Select	ENSP00000310721.3:p.Lys50=
ENST00000310193.3:c.150A>G	ENSP00000310721.3:p.Lys50=
NM_004820.3:c.150A>G	NP_004811.1:p.Lys50=
NM_001324112.1:c.150A>G	NP_001311041.1:p.Lys50=
NM_004820.4:c.150A>G	NP_004811.1:p.Lys50=
XM_017014002.1:c.216A>G	XP_016869491.1:p.Lys72=
NM_004820.5:c.150A>G MANE Select	NP_004811.1:p.Lys50=
NM_001324112.2:c.150A>G	NP_001311041.1:p.Lys50=