Canonical Allele Identifier: CA461121077
Gene: CYP7B1 HGNC NCBI

Linked Data

gnomAD v4: 8-64624497-A-G
MyVariant Identifiers: chr8:g.65537054A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624497A>G , CM000670.2:g.64624497A>G GRCh38
NC_000008.10:g.65537054A>G , CM000670.1:g.65537054A>G GRCh37
NC_000008.9:g.65699608A>G NCBI36
NG_008338.1:g.179295T>C
NG_008338.2:g.179295T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000310193.4:c.165T>C MANE Select ENSP00000310721.3:p.Tyr55=
ENST00000310193.3:c.165T>C ENSP00000310721.3:p.Tyr55=
NM_004820.3:c.165T>C NP_004811.1:p.Tyr55=
NM_001324112.1:c.165T>C NP_001311041.1:p.Tyr55=
NM_004820.4:c.165T>C NP_004811.1:p.Tyr55=
XM_017014002.1:c.231T>C XP_016869491.1:p.Tyr77=
NM_004820.5:c.165T>C MANE Select NP_004811.1:p.Tyr55=
NM_001324112.2:c.165T>C NP_001311041.1:p.Tyr55=