Canonical Allele Identifier: CA1085457042
Gene: FAM50B HGNC NCBI

Linked Data

dbSNP Id: rs1761992713
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836916C>T , CM000668.2:g.3836916C>T GRCh38
NC_000006.11:g.3837150C>T , CM000668.1:g.3837150C>T GRCh37
NC_000006.10:g.3782149C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4905C>T XP_016866218.1:n.-24+4905C>T
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Search 100 bp 3'