Canonical Allele Identifier: CA371334089

Gene: CYP7B1

Linked Data

• gnomAD v4: 8-64604730-G-C
• MyVariant Identifiers: chr8:g.65517287G>C (hg19) ; chr8:g.64604730G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64604730G>C , CM000670.2:g.64604730G>C	GRCh38
NC_000008.10:g.65517287G>C , CM000670.1:g.65517287G>C	GRCh37
NC_000008.9:g.65679841G>C	NCBI36
NG_008338.1:g.199062C>G
NG_008338.2:g.199062C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310193.4:c.1185C>G MANE Select	ENSP00000310721.3:p.Ile395Met
ENST00000310193.3:c.1185C>G	ENSP00000310721.3:p.Ile395Met
ENST00000523954.1:n.459C>G
NM_004820.3:c.1185C>G	NP_004811.1:p.Ile395Met
NM_001324112.1:c.1185C>G	NP_001311041.1:p.Ile395Met
NM_004820.4:c.1185C>G	NP_004811.1:p.Ile395Met
XM_017014002.1:c.1251C>G	XP_016869491.1:p.Ile417Met
NM_004820.5:c.1185C>G MANE Select	NP_004811.1:p.Ile395Met
NM_001324112.2:c.1185C>G	NP_001311041.1:p.Ile395Met