Canonical Allele Identifier: CA2610262435
Gene:

Linked Data

gnomAD v4: 10-94762612-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762612C>A , CM000672.2:g.94762612C>A GRCh38
NC_000010.10:g.96522369C>A , CM000672.1:g.96522369C>A GRCh37
NC_000010.9:g.96512359C>A NCBI36
NG_008384.2:g.4907C>A
NG_008384.3:g.4932C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000464755.1:c.932-12446C>A ENSP00000483243.1:n.932-12446C>A
Search 100 bp 5'
Search 100 bp 3'