Canonical Allele Identifier: CA826060546

Gene: HMGCLL1

Linked Data

• dbSNP Id: rs954938240
• gnomAD v3: 6-55608497-C-G
• gnomAD v4: 6-55608497-C-G
• MyVariant Identifiers: chr6:g.55473295C>G (hg19) ; chr6:g.55608497C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.55608497C>G , CM000668.2:g.55608497C>G	GRCh38
NC_000006.11:g.55473295C>G , CM000668.1:g.55473295C>G	GRCh37
NC_000006.10:g.55581254C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011514701.1:c.-279-66357G>C	XP_011513003.1:n.-279-66357G>C