Canonical Allele Identifier: CA461121087
Gene: CYP7B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.65537057A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624500A>T , CM000670.2:g.64624500A>T GRCh38
NC_000008.10:g.65537057A>T , CM000670.1:g.65537057A>T GRCh37
NC_000008.9:g.65699611A>T NCBI36
NG_008338.1:g.179292T>A
NG_008338.2:g.179292T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000310193.4:c.162T>A MANE Select ENSP00000310721.3:p.Pro54=
ENST00000310193.3:c.162T>A ENSP00000310721.3:p.Pro54=
NM_004820.3:c.162T>A NP_004811.1:p.Pro54=
NM_001324112.1:c.162T>A NP_001311041.1:p.Pro54=
NM_004820.4:c.162T>A NP_004811.1:p.Pro54=
XM_017014002.1:c.228T>A XP_016869491.1:p.Pro76=
NM_004820.5:c.162T>A MANE Select NP_004811.1:p.Pro54=
NM_001324112.2:c.162T>A NP_001311041.1:p.Pro54=