Canonical Allele Identifier: CA1321609183
Gene: FAM117B HGNC NCBI

Linked Data

dbSNP Id: rs11694172
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202667581A>T , CM000664.2:g.202667581A>T GRCh38
NC_000002.11:g.203532304A>T , CM000664.1:g.203532304A>T GRCh37
NC_000002.10:g.203240549A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392238.3:c.602-28300A>T MANE Select ENSP00000376071.2:n.602-28300A>T
ENST00000392238.2:c.602-28300A>T ENSP00000376071.2:n.602-28300A>T
ENST00000481658.1:n.301-28300A>T
NM_173511.3:c.602-28300A>T NP_775782.2:n.602-28300A>T
NM_173511.4:c.602-28300A>T MANE Select NP_775782.2:n.602-28300A>T
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