Canonical Allele Identifier: CA156094605

Gene:

Linked Data

• dbSNP Id: rs1032050014
• MyVariant Identifiers: chr7:g.30937263C>T (hg19) ; chr7:g.30897648C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30897648C>T , CM000669.2:g.30897648C>T	GRCh38
NC_000007.13:g.30937263C>T , CM000669.1:g.30937263C>T	GRCh37
NC_000007.12:g.30903788C>T	NCBI36
NG_007475.2:g.49255C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509504.2:c.622-14345C>T