Canonical Allele Identifier: CA21327507
Gene:

Linked Data

dbSNP Id: rs150808643
gnomAD v2: 1-38633765-C-T
gnomAD v3: 1-38168093-C-T
gnomAD v4: 1-38168093-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.38168093C>T , CM000663.2:g.38168093C>T GRCh38
NC_000001.10:g.38633765C>T , CM000663.1:g.38633765C>T GRCh37
NC_000001.9:g.38406352C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947202.1:n.175+6270C>T
XR_947203.1:n.62-24912C>T
XR_947204.1:n.175+6270C>T
XR_947205.1:n.175+6270C>T
XR_001737984.1:n.175+6270C>T
XR_001737985.1:n.62-24912C>T
XR_001737986.1:n.175+6270C>T
XR_001737987.1:n.175+6270C>T
XR_002958294.1:n.175+6270C>T
XR_947205.2:n.175+6270C>T