Canonical Allele Identifier: CA789337390

Gene:

Linked Data

• dbSNP Id: rs1163518842
• gnomAD v3: 4-153943613-A-G
• gnomAD v4: 4-153943613-A-G
• MyVariant Identifiers: chr4:g.154864765A>G (hg19) ; chr4:g.153943613A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153943613A>G , CM000666.2:g.153943613A>G	GRCh38
NC_000004.11:g.154864765A>G , CM000666.1:g.154864765A>G	GRCh37
NC_000004.10:g.155084215A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001741892.1:n.1348-5208A>G