Canonical Allele Identifier: CA820839201
Gene:

Linked Data

dbSNP Id: rs1196432587
MyVariant Identifiers: chr6:g.151954742G>A (hg19) chr6:g.151633607G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633607G>A , CM000668.2:g.151633607G>A GRCh38
NC_000006.11:g.151954742G>A , CM000668.1:g.151954742G>A GRCh37
NC_000006.10:g.151996435G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3625G>A
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