Canonical Allele Identifier: CA837138541
Gene:

Linked Data

dbSNP Id: rs1455694696
gnomAD v3: 7-26605807-T-G
gnomAD v4: 7-26605807-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26605807T>G , CM000669.2:g.26605807T>G GRCh38
NC_000007.13:g.26645426T>G , CM000669.1:g.26645426T>G GRCh37
NC_000007.12:g.26611951T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927131.1:n.1118-6437A>C
XR_927131.2:n.1186-6437A>C