Canonical Allele Identifier: CA371338793

Gene: CYP7B1

Linked Data

• ClinVar Variation Id: 2843995
• ClinVar RCV Id: RCV003752189
• MyVariant Identifiers: chr8:g.65537050C>A (hg19) ; chr8:g.64624493C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64624493C>A , CM000670.2:g.64624493C>A	GRCh38
NC_000008.10:g.65537050C>A , CM000670.1:g.65537050C>A	GRCh37
NC_000008.9:g.65699604C>A	NCBI36
NG_008338.1:g.179299G>T
NG_008338.2:g.179299G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000310193.4:c.169G>T MANE Select	ENSP00000310721.3:p.Gly57Ter
ENST00000310193.3:c.169G>T	ENSP00000310721.3:p.Gly57Ter
NM_004820.3:c.169G>T	NP_004811.1:p.Gly57Ter
NM_001324112.1:c.169G>T	NP_001311041.1:p.Gly57Ter
NM_004820.4:c.169G>T	NP_004811.1:p.Gly57Ter
XM_017014002.1:c.235G>T	XP_016869491.1:p.Gly79Ter
NM_004820.5:c.169G>T MANE Select	NP_004811.1:p.Gly57Ter
NM_001324112.2:c.169G>T	NP_001311041.1:p.Gly57Ter