Canonical Allele Identifier: CA805749873
Gene:

Linked Data

dbSNP Id: rs1338900442
MyVariant Identifiers: chr5:g.151734177T>C (hg19) chr5:g.152354616T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.152354616T>C , CM000667.2:g.152354616T>C GRCh38
NC_000005.9:g.151734177T>C , CM000667.1:g.151734177T>C GRCh37
NC_000005.8:g.151714370T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944433.1:n.196+16753T>C
XR_944433.2:n.197+16753T>C
Search 100 bp 5'
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