Canonical Allele Identifier: CA144309900
Gene:

Linked Data

dbSNP Id: rs760468176
gnomAD v2: 6-98462608-C-T
gnomAD v3: 6-98014732-C-T
gnomAD v4: 6-98014732-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014732C>T , CM000668.2:g.98014732C>T GRCh38
NC_000006.11:g.98462608C>T , CM000668.1:g.98462608C>T GRCh37
NC_000006.10:g.98569329C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.371+45266C>T
XR_942809.1:n.371+45266C>T