Canonical Allele Identifier: CA799753609
Gene:

Linked Data

dbSNP Id: rs1306440710
gnomAD v3: 4-89655979-C-A
gnomAD v4: 4-89655979-C-A
MyVariant Identifiers: chr4:g.90577130C>A (hg19) chr4:g.89655979C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89655979C>A , CM000666.2:g.89655979C>A GRCh38
NC_000004.11:g.90577130C>A , CM000666.1:g.90577130C>A GRCh37
NC_000004.10:g.90796153C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+28062C>A
XR_938987.1:n.688+28062C>A
XR_938988.1:n.554+28062C>A
XR_938990.1:n.299-35306C>A
XR_938991.1:n.434+28062C>A
XR_938994.1:n.779+28062C>A
XR_938995.1:n.613+28062C>A
XR_938986.2:n.459+28062C>A
XR_938987.2:n.748+28062C>A
Search 100 bp 5'
Search 100 bp 3'