Canonical Allele Identifier: CA461422281

Gene: CYP7B1

Linked Data

• MyVariant Identifiers: chr8:g.65528780A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64616223A>G , CM000670.2:g.64616223A>G	GRCh38
NC_000008.10:g.65528780A>G , CM000670.1:g.65528780A>G	GRCh37
NC_000008.9:g.65691334A>G	NCBI36
NG_008338.1:g.187569T>C
NG_008338.2:g.187569T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310193.4:c.318T>C MANE Select	ENSP00000310721.3:p.His106=
ENST00000310193.3:c.318T>C	ENSP00000310721.3:p.His106=
NM_004820.3:c.318T>C	NP_004811.1:p.His106=
NM_001324112.1:c.318T>C	NP_001311041.1:p.His106=
NM_004820.4:c.318T>C	NP_004811.1:p.His106=
XM_017014002.1:c.384T>C	XP_016869491.1:p.His128=
NM_004820.5:c.318T>C MANE Select	NP_004811.1:p.His106=
NM_001324112.2:c.318T>C	NP_001311041.1:p.His106=