Canonical Allele Identifier: CA307005664
Gene:

Linked Data

dbSNP Id: rs763609453
MyVariant Identifiers: chr19:g.29035363A>G (hg19) chr19:g.28544456A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544456A>G , CM000681.2:g.28544456A>G GRCh38
NC_000019.9:g.29035363A>G , CM000681.1:g.29035363A>G GRCh37
NC_000019.8:g.33727203A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110759.1:n.657-77676T>C
XR_243979.1:n.110-51433T>C
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