Canonical Allele Identifier: CA1138946835
Gene:

Linked Data

dbSNP Id: rs2015451132
gnomAD v3: Y-8734436-C-T
gnomAD v4: Y-8734436-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8734436C>T , CM000686.2:g.8734436C>T GRCh38
NC_000024.9:g.8602477C>T , CM000686.1:g.8602477C>T GRCh37
NC_000024.8:g.8662477C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000623558.1:c.197-5394C>T ENSP00000485446.1:n.197-5394C>T
ENST00000624237.1:c.64-7619C>T ENSP00000485137.1:n.64-7619C>T
ENST00000624593.1:c.-57+14280G>A ENSP00000485106.1:n.-57+14280G>A