Canonical Allele Identifier: CA823881892
Gene:

Linked Data

dbSNP Id: rs1489714586
MyVariant Identifiers: chr6:g.31407569A>T (hg19) chr6:g.31439792A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439792A>T , CM000668.2:g.31439792A>T GRCh38
NC_000006.11:g.31407569A>T , CM000668.1:g.31407569A>T GRCh37
NC_000006.10:g.31515548A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.315T>A
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