Canonical Allele Identifier: CA1138998444
Gene:

Linked Data

gnomAD v3: Y-8556222-C-T
gnomAD v4: Y-8556222-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8556222C>T , CM000686.2:g.8556222C>T GRCh38
NC_000024.9:g.8424263C>T , CM000686.1:g.8424263C>T GRCh37
NC_000024.8:g.8484263C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000624593.1:c.*23-6427G>A ENSP00000485106.1:n.*23-6427G>A