Canonical Allele Identifier: CA1138946816
Gene:

Linked Data

dbSNP Id: rs2015451043
gnomAD v3: Y-8734352-G-T
gnomAD v4: Y-8734352-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8734352G>T , CM000686.2:g.8734352G>T GRCh38
NC_000024.9:g.8602393G>T , CM000686.1:g.8602393G>T GRCh37
NC_000024.8:g.8662393G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000623558.1:c.197-5478G>T ENSP00000485446.1:n.197-5478G>T
ENST00000624237.1:c.64-7703G>T ENSP00000485137.1:n.64-7703G>T
ENST00000624593.1:c.-57+14364C>A ENSP00000485106.1:n.-57+14364C>A