Canonical Allele Identifier: CA1110104823
Gene:

Linked Data

dbSNP Id: rs1798579153
gnomAD v3: 8-5907450-T-C
gnomAD v4: 8-5907450-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907450T>C , CM000670.2:g.5907450T>C GRCh38
NC_000008.10:g.5764972T>C , CM000670.1:g.5764972T>C GRCh37
NC_000008.9:g.5752380T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941374.1:n.308-7719A>G
XR_941375.1:n.308-7719A>G
XR_941376.1:n.406-7719A>G
XR_941377.1:n.308-7719A>G
XR_941378.1:n.216-7719A>G
XR_001745765.1:n.308-7719A>G
XR_001745766.1:n.406-7719A>G
XR_001745767.1:n.216-7719A>G
XR_001745768.1:n.308-7719A>G
XR_941374.2:n.308-7719A>G
XR_941375.2:n.308-7719A>G