Canonical Allele Identifier: CA171706464
Gene:

Linked Data

dbSNP Id: rs555303796
gnomAD v2: 8-5765038-G-C
gnomAD v3: 8-5907516-G-C
gnomAD v4: 8-5907516-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.5907516G>C , CM000670.2:g.5907516G>C GRCh38
NC_000008.10:g.5765038G>C , CM000670.1:g.5765038G>C GRCh37
NC_000008.9:g.5752446G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941374.1:n.308-7785C>G
XR_941375.1:n.308-7785C>G
XR_941376.1:n.406-7785C>G
XR_941377.1:n.308-7785C>G
XR_941378.1:n.216-7785C>G
XR_001745765.1:n.308-7785C>G
XR_001745766.1:n.406-7785C>G
XR_001745767.1:n.216-7785C>G
XR_001745768.1:n.308-7785C>G
XR_941374.2:n.308-7785C>G
XR_941375.2:n.308-7785C>G