Canonical Allele Identifier: CA2579176612
Gene: CYP7B1 HGNC NCBI

Linked Data

gnomAD v4: 8-64624556-A-AG
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624556_64624557insG , CM000670.2:g.64624556_64624557insG GRCh38
NC_000008.10:g.65537113_65537114insG , CM000670.1:g.65537113_65537114insG GRCh37
NC_000008.9:g.65699667_65699668insG NCBI36
NG_008338.1:g.179235_179236insC
NG_008338.2:g.179235_179236insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.123-18_123-17insC MANE Select ENSP00000310721.3:n.123-18_123-17insC
ENST00000310193.3:c.123-18_123-17insC ENSP00000310721.3:n.123-18_123-17insC
NM_004820.3:c.123-18_123-17insC NP_004811.1:n.123-18_123-17insC
NM_001324112.1:c.123-18_123-17insC NP_001311041.1:n.123-18_123-17insC
NM_004820.4:c.123-18_123-17insC NP_004811.1:n.123-18_123-17insC
XM_017014002.1:c.189-18_189-17insC XP_016869491.1:n.189-18_189-17insC
NM_004820.5:c.123-18_123-17insC MANE Select NP_004811.1:n.123-18_123-17insC
NM_001324112.2:c.123-18_123-17insC NP_001311041.1:n.123-18_123-17insC
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