Canonical Allele Identifier: CA156094534

Gene:

Linked Data

• dbSNP Id: rs1010653406
• MyVariant Identifiers: chr7:g.30937229C>G (hg19) ; chr7:g.30897614C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30897614C>G , CM000669.2:g.30897614C>G	GRCh38
NC_000007.13:g.30937229C>G , CM000669.1:g.30937229C>G	GRCh37
NC_000007.12:g.30903754C>G	NCBI36
NG_007475.2:g.49221C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000509504.2:c.622-14379C>G