Canonical Allele Identifier: CA997806895
Gene:

Linked Data

dbSNP Id: rs1644376543
gnomAD v3: 1-2567434-C-T
gnomAD v4: 1-2567434-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2567434C>T , CM000663.2:g.2567434C>T GRCh38
NC_000001.10:g.2498873C>T , CM000663.1:g.2498873C>T GRCh37
NC_000001.9:g.2475545G>A NCBI36
NG_047096.1:g.16070C>T

Transcript Alleles

HGVS Amino-acid Change
NR_121638.1:n.71+829C>T