Canonical Allele Identifier: CA307005690
Gene:

Linked Data

dbSNP Id: rs1010228687
gnomAD v3: 19-28544653-C-T
gnomAD v4: 19-28544653-C-T
MyVariant Identifiers: chr19:g.29035560C>T (hg19) chr19:g.28544653C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544653C>T , CM000681.2:g.28544653C>T GRCh38
NC_000019.9:g.29035560C>T , CM000681.1:g.29035560C>T GRCh37
NC_000019.8:g.33727400C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110759.1:n.657-77873G>A
XR_243979.1:n.110-51630G>A
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