Canonical Allele Identifier: CA15460028
Gene:

Linked Data

dbSNP Id: rs1528983
gnomAD v2: 6-91544513-T-C
gnomAD v3: 6-90834795-T-C
gnomAD v4: 6-90834795-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.90834795T>C , CM000668.2:g.90834795T>C GRCh38
NC_000006.11:g.91544513T>C , CM000668.1:g.91544513T>C GRCh37
NC_000006.10:g.91601234T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744259.1:n.1244-73261T>C