Canonical Allele Identifier: CA289219349
Gene:

Linked Data

dbSNP Id: rs930739273
MyVariant Identifiers: chr17:g.27703396A>T (hg19) chr17:g.29376378A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29376378A>T , CM000679.2:g.29376378A>T GRCh38
NC_000017.10:g.27703396A>T , CM000679.1:g.27703396A>T GRCh37
NC_000017.9:g.24727522A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011525588.1:c.1008-6073T>A XP_011523890.1:n.1008-6073T>A
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