Canonical Allele Identifier: CA41419432
Gene:

Linked Data

dbSNP Id: rs914562130
gnomAD v2: 2-1557848-C-T
gnomAD v3: 2-1554076-C-T
gnomAD v4: 2-1554076-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1554076C>T , CM000664.2:g.1554076C>T GRCh38
NC_000002.11:g.1557848C>T , CM000664.1:g.1557848C>T GRCh37
NC_000002.10:g.1536855C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011510447.1:c.-1097C>T XP_011508749.1:n.-1097C>T
XM_011510448.1:c.-1097C>T XP_011508750.1:n.-1097C>T
XR_922720.1:n.85+2422G>A
XM_017005455.1:c.-1097C>T XP_016860944.1:n.-1097C>T
NR_168373.1:n.746-94C>T