Canonical Allele Identifier: CA144309866
Gene:

Linked Data

dbSNP Id: rs187369582
gnomAD v2: 6-98462303-C-T
gnomAD v3: 6-98014427-C-T
gnomAD v4: 6-98014427-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014427C>T , CM000668.2:g.98014427C>T GRCh38
NC_000006.11:g.98462303C>T , CM000668.1:g.98462303C>T GRCh37
NC_000006.10:g.98569024C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+44961C>T
XR_942809.1:n.371+44961C>T