Canonical Allele Identifier: CA2668425489
Gene: SI HGNC NCBI

Linked Data

gnomAD v4: 3-165068925-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165068925G>T , CM000665.2:g.165068925G>T GRCh38
NC_000003.11:g.164786713G>T , CM000665.1:g.164786713G>T GRCh37
NC_000003.10:g.166269407G>T NCBI36
NG_017043.1:g.14571C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264382.8:c.374-94C>A MANE Select ENSP00000264382.3:n.374-94C>A
ENST00000264382.7:c.374-94C>A ENSP00000264382.3:n.374-94C>A
ENST00000476593.1:c.*249-94C>A ENSP00000419450.1:n.*249-94C>A
NM_001041.3:c.374-94C>A NP_001032.2:n.374-94C>A
XM_011513078.1:c.275-94C>A XP_011511380.1:n.275-94C>A
XM_011513078.2:c.275-94C>A XP_011511380.1:n.275-94C>A
NM_001041.4:c.374-94C>A MANE Select NP_001032.2:n.374-94C>A
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