Canonical Allele Identifier: CA150162941
Gene:

Linked Data

dbSNP Id: rs1032980834
MyVariant Identifiers: chr6:g.151954795G>A (hg19) chr6:g.151633660G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633660G>A , CM000668.2:g.151633660G>A GRCh38
NC_000006.11:g.151954795G>A , CM000668.1:g.151954795G>A GRCh37
NC_000006.10:g.151996488G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943115.1:n.2496+3678G>A
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