Canonical Allele Identifier: CA308543673
Gene:

Linked Data

dbSNP Id: rs543553627
MyVariant Identifiers: chr19:g.42152187del (hg19) chr19:g.41648266del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41648267del , CM000681.2:g.41648267del GRCh38
NC_000019.9:g.42152188del , CM000681.1:g.42152188del GRCh37
NC_000019.8:g.46844028del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935972.1:n.170+3236del
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