Canonical Allele Identifier: CA1110104829
Gene:

Linked Data

dbSNP Id: rs1798579301
gnomAD v3: 8-5907457-A-G
gnomAD v4: 8-5907457-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907457A>G , CM000670.2:g.5907457A>G GRCh38
NC_000008.10:g.5764979A>G , CM000670.1:g.5764979A>G GRCh37
NC_000008.9:g.5752387A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941374.1:n.308-7726T>C
XR_941375.1:n.308-7726T>C
XR_941376.1:n.406-7726T>C
XR_941377.1:n.308-7726T>C
XR_941378.1:n.216-7726T>C
XR_001745765.1:n.308-7726T>C
XR_001745766.1:n.406-7726T>C
XR_001745767.1:n.216-7726T>C
XR_001745768.1:n.308-7726T>C
XR_941374.2:n.308-7726T>C
XR_941375.2:n.308-7726T>C