Canonical Allele Identifier: CA1823684570
Gene: FAM135B HGNC NCBI

Linked Data

dbSNP Id: rs11166827
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.138492027C>G , CM000670.2:g.138492027C>G GRCh38
NC_000008.10:g.139504270C>G , CM000670.1:g.139504270C>G GRCh37
NC_000008.9:g.139573452C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395297.6:c.-20+4644G>C MANE Select ENSP00000378710.1:n.-20+4644G>C
ENST00000276737.10:c.-20+4644G>C ENSP00000276737.6:n.-20+4644G>C
ENST00000395297.5:c.-20+4644G>C ENSP00000378710.1:n.-20+4644G>C
NM_015912.3:c.-20+4644G>C NP_056996.2:n.-20+4644G>C
XM_011517061.1:c.-165+4644G>C XP_011515363.1:n.-165+4644G>C
XM_011517062.1:c.-20+4644G>C XP_011515364.1:n.-20+4644G>C
NM_001362965.1:c.-20+5600G>C NP_001349894.1:n.-20+5600G>C
XM_011517061.2:c.-165+4644G>C XP_011515363.1:n.-165+4644G>C
NM_015912.4:c.-20+4644G>C MANE Select NP_056996.2:n.-20+4644G>C
NM_001362965.2:c.-20+5600G>C NP_001349894.1:n.-20+5600G>C
Search 100 bp 5'
Search 100 bp 3'