Canonical Allele Identifier: CA1649498192
Gene:

Linked Data

dbSNP Id: rs1772156632
gnomAD v3: 6-98014615-A-T
gnomAD v4: 6-98014615-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014615A>T , CM000668.2:g.98014615A>T GRCh38
NC_000006.11:g.98462491A>T , CM000668.1:g.98462491A>T GRCh37
NC_000006.10:g.98569212A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+45149A>T
XR_942809.1:n.371+45149A>T