Canonical Allele Identifier: CA553236619
Gene:

Linked Data

dbSNP Id: rs1257349665
gnomAD v2: 4-90577046-C-T
gnomAD v3: 4-89655895-C-T
gnomAD v4: 4-89655895-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89655895C>T , CM000666.2:g.89655895C>T GRCh38
NC_000004.11:g.90577046C>T , CM000666.1:g.90577046C>T GRCh37
NC_000004.10:g.90796069C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+27978C>T
XR_938987.1:n.688+27978C>T
XR_938988.1:n.554+27978C>T
XR_938990.1:n.299-35390C>T
XR_938991.1:n.434+27978C>T
XR_938994.1:n.779+27978C>T
XR_938995.1:n.613+27978C>T
XR_938986.2:n.459+27978C>T
XR_938987.2:n.748+27978C>T