Canonical Allele Identifier: CA1052367776

Gene: USF3

Linked Data

• dbSNP Id: rs1947254918
• gnomAD v3: 3-113651166-C-G
• gnomAD v4: 3-113651166-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.113651166C>G , CM000665.2:g.113651166C>G	GRCh38
NC_000003.11:g.113370013C>G , CM000665.1:g.113370013C>G	GRCh37
NC_000003.10:g.114852703C>G	NCBI36
NG_055006.1:g.50492G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000316407.9:c.*3778G>C MANE Select	ENSP00000320794.4:n.*3778G>C
ENST00000316407.8:c.*3778G>C	ENSP00000320794.4:n.*3778G>C
ENST00000491165.5:c.257-1316G>C	ENSP00000420752.1:n.257-1316G>C
NM_001009899.3:c.*3778G>C	NP_001009899.3:n.*3778G>C
NR_111981.1:n.668-1316G>C
XM_005247208.3:c.*3778G>C	XP_005247265.2:n.*3778G>C
XM_005247208.4:c.*3778G>C	XP_005247265.2:n.*3778G>C
XM_017005871.1:c.*3778G>C	XP_016861360.1:n.*3778G>C
XM_017005872.1:c.*3778G>C	XP_016861361.1:n.*3778G>C
XM_024453391.1:c.*3778G>C	XP_024309159.1:n.*3778G>C
XM_024453392.1:c.*3778G>C	XP_024309160.1:n.*3778G>C
NM_001009899.4:c.*3778G>C MANE Select	NP_001009899.3:n.*3778G>C
NR_111981.2:n.664-1316G>C