Canonical Allele Identifier: CA824452247
Gene: FAM50B HGNC NCBI

Linked Data

dbSNP Id: rs1304126832
MyVariant Identifiers: chr6:g.3837233T>A (hg19) chr6:g.3836999T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836999T>A , CM000668.2:g.3836999T>A GRCh38
NC_000006.11:g.3837233T>A , CM000668.1:g.3837233T>A GRCh37
NC_000006.10:g.3782232T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4988T>A XP_016866218.1:n.-24+4988T>A
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