Canonical Allele Identifier: CA1606874700
Gene: FAM50B HGNC NCBI

Linked Data

dbSNP Id: rs1761992510

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3836906_3836907insT , CM000668.2:g.3836906_3836907insT GRCh38
NC_000006.11:g.3837140_3837141insT , CM000668.1:g.3837140_3837141insT GRCh37
NC_000006.10:g.3782139_3782140insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010729.1:c.-24+4895_-24+4896insT XP_016866218.1:n.-24+4895_-24+4896insT