Canonical Allele Identifier: CA705306329
Gene:

Linked Data

dbSNP Id: rs903282363
gnomAD v3: 14-36384822-G-T
gnomAD v4: 14-36384822-G-T
MyVariant Identifiers: chr14:g.36854027G>T (hg19) chr14:g.36384822G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384822G>T , CM000676.2:g.36384822G>T GRCh38
NC_000014.8:g.36854027G>T , CM000676.1:g.36854027G>T GRCh37
NC_000014.7:g.35923778G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537428.1:c.319-12337G>T XP_011535730.1:n.319-12337G>T
XR_943756.1:n.358+23726G>T
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