Canonical Allele Identifier: CA2711069945
Gene: FAM50B HGNC NCBI

Linked Data

dbSNP Id: rs2127616342
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3837016G>A , CM000668.2:g.3837016G>A GRCh38
NC_000006.11:g.3837250G>A , CM000668.1:g.3837250G>A GRCh37
NC_000006.10:g.3782249G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+5005G>A XP_016866218.1:n.-24+5005G>A
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