Canonical Allele Identifier: CA134049597
Gene:

Linked Data

dbSNP Id: rs193083931
gnomAD v2: 6-8525437-C-T
gnomAD v3: 6-8525204-C-T
gnomAD v4: 6-8525204-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525204C>T , CM000668.2:g.8525204C>T GRCh38
NC_000006.11:g.8525437C>T , CM000668.1:g.8525437C>T GRCh37
NC_000006.10:g.8470436C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038979.1:n.626-33381C>T
NR_038980.1:n.649-33381C>T