Canonical Allele Identifier: CA371338144

Gene: CYP7B1

Linked Data

• MyVariant Identifiers: chr8:g.65536958A>T (hg19) ; chr8:g.64624401A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64624401A>T , CM000670.2:g.64624401A>T	GRCh38
NC_000008.10:g.65536958A>T , CM000670.1:g.65536958A>T	GRCh37
NC_000008.9:g.65699512A>T	NCBI36
NG_008338.1:g.179391T>A
NG_008338.2:g.179391T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.259+2T>A MANE Select	ENSP00000310721.3:n.259+2T>A
ENST00000310193.3:c.259+2T>A	ENSP00000310721.3:n.259+2T>A
NM_004820.3:c.259+2T>A	NP_004811.1:n.259+2T>A
NM_001324112.1:c.259+2T>A	NP_001311041.1:n.259+2T>A
NM_004820.4:c.259+2T>A	NP_004811.1:n.259+2T>A
XM_017014002.1:c.325+2T>A	XP_016869491.1:n.325+2T>A
NM_004820.5:c.259+2T>A MANE Select	NP_004811.1:n.259+2T>A
NM_001324112.2:c.259+2T>A	NP_001311041.1:n.259+2T>A