Canonical Allele Identifier: CA187073553

Gene: FAM135B

Linked Data

• dbSNP Id: rs1038298018
• gnomAD v3: 8-138491986-G-A
• gnomAD v4: 8-138491986-G-A
• MyVariant Identifiers: chr8:g.139504229G>A (hg19) ; chr8:g.138491986G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.138491986G>A , CM000670.2:g.138491986G>A	GRCh38
NC_000008.10:g.139504229G>A , CM000670.1:g.139504229G>A	GRCh37
NC_000008.9:g.139573411G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395297.6:c.-20+4685C>T MANE Select	ENSP00000378710.1:n.-20+4685C>T
ENST00000276737.10:c.-20+4685C>T	ENSP00000276737.6:n.-20+4685C>T
ENST00000395297.5:c.-20+4685C>T	ENSP00000378710.1:n.-20+4685C>T
NM_015912.3:c.-20+4685C>T	NP_056996.2:n.-20+4685C>T
XM_011517061.1:c.-165+4685C>T	XP_011515363.1:n.-165+4685C>T
XM_011517062.1:c.-20+4685C>T	XP_011515364.1:n.-20+4685C>T
NM_001362965.1:c.-20+5641C>T	NP_001349894.1:n.-20+5641C>T
XM_011517061.2:c.-165+4685C>T	XP_011515363.1:n.-165+4685C>T
NM_015912.4:c.-20+4685C>T MANE Select	NP_056996.2:n.-20+4685C>T
NM_001362965.2:c.-20+5641C>T	NP_001349894.1:n.-20+5641C>T