Canonical Allele Identifier: CA690762864
Gene:

Linked Data

dbSNP Id: rs1304677726
MyVariant Identifiers: chr12:g.6385782G>A (hg19) chr12:g.6276616G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6276616G>A , CM000674.2:g.6276616G>A GRCh38
NC_000012.11:g.6385782G>A , CM000674.1:g.6385782G>A GRCh37
NC_000012.10:g.6256043G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001748976.1:n.157+16483C>T
XR_001748977.1:n.157+16483C>T
XR_001748978.1:n.157+16483C>T
XR_001748979.1:n.157+16483C>T
XR_001748980.1:n.157+16483C>T
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