Canonical Allele Identifier: CA187073548

Gene: FAM135B

Linked Data

• dbSNP Id: rs1051974609
• gnomAD v3: 8-138491941-G-C
• gnomAD v4: 8-138491941-G-C
• MyVariant Identifiers: chr8:g.139504184G>C (hg19) ; chr8:g.138491941G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.138491941G>C , CM000670.2:g.138491941G>C	GRCh38
NC_000008.10:g.139504184G>C , CM000670.1:g.139504184G>C	GRCh37
NC_000008.9:g.139573366G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000395297.6:c.-20+4730C>G MANE Select	ENSP00000378710.1:n.-20+4730C>G
ENST00000276737.10:c.-20+4730C>G	ENSP00000276737.6:n.-20+4730C>G
ENST00000395297.5:c.-20+4730C>G	ENSP00000378710.1:n.-20+4730C>G
NM_015912.3:c.-20+4730C>G	NP_056996.2:n.-20+4730C>G
XM_011517061.1:c.-165+4730C>G	XP_011515363.1:n.-165+4730C>G
XM_011517062.1:c.-20+4730C>G	XP_011515364.1:n.-20+4730C>G
NM_001362965.1:c.-20+5686C>G	NP_001349894.1:n.-20+5686C>G
XM_011517061.2:c.-165+4730C>G	XP_011515363.1:n.-165+4730C>G
NM_015912.4:c.-20+4730C>G MANE Select	NP_056996.2:n.-20+4730C>G
NM_001362965.2:c.-20+5686C>G	NP_001349894.1:n.-20+5686C>G