Canonical Allele Identifier: CA150162772

Gene:

Linked Data

• dbSNP Id: rs554137524
• gnomAD v2: 6-151954540-G-C
• gnomAD v3: 6-151633405-G-C
• gnomAD v4: 6-151633405-G-C
• MyVariant Identifiers: chr6:g.151954540G>C (hg19) ; chr6:g.151633405G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633405G>C , CM000668.2:g.151633405G>C	GRCh38
NC_000006.11:g.151954540G>C , CM000668.1:g.151954540G>C	GRCh37
NC_000006.10:g.151996233G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3423G>C