Canonical Allele Identifier: CA2614496194
Gene:

Linked Data

gnomAD v4: 11-66510603-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66510603G>C , CM000673.2:g.66510603G>C GRCh38
NC_000011.9:g.66278074G>C , CM000673.1:g.66278074G>C GRCh37
NC_000011.8:g.66034650G>C NCBI36
NG_009093.1:g.4956G>C
NG_032068.1:g.35195G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000419755.3:c.159-410G>C ENSP00000398526.3:n.159-410G>C
Search 100 bp 5'
Search 100 bp 3'