Canonical Allele Identifier: CA603107854
Gene:

Linked Data

dbSNP Id: rs1439909847
gnomAD v2: 12-6385729-T-G
gnomAD v3: 12-6276563-T-G
gnomAD v4: 12-6276563-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6276563T>G , CM000674.2:g.6276563T>G GRCh38
NC_000012.11:g.6385729T>G , CM000674.1:g.6385729T>G GRCh37
NC_000012.10:g.6255990T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001748976.1:n.157+16536A>C
XR_001748977.1:n.157+16536A>C
XR_001748978.1:n.157+16536A>C
XR_001748979.1:n.157+16536A>C
XR_001748980.1:n.157+16536A>C