Canonical Allele Identifier: CA150159459

Gene:

Linked Data

• dbSNP Id: rs917377265
• gnomAD v2: 6-151948415-G-T
• gnomAD v3: 6-151627280-G-T
• gnomAD v4: 6-151627280-G-T
• MyVariant Identifiers: chr6:g.151948415G>T (hg19) ; chr6:g.151627280G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151627280G>T , CM000668.2:g.151627280G>T	GRCh38
NC_000006.11:g.151948415G>T , CM000668.1:g.151948415G>T	GRCh37
NC_000006.10:g.151990108G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943113.1:n.706G>T
XR_943115.1:n.706G>T