Canonical Allele Identifier: CA2687439989

Gene: GGH

Linked Data

• gnomAD v4: 8-63038807-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038807G>C , CM000670.2:g.63038807G>C	GRCh38
NC_000008.10:g.63951366G>C , CM000670.1:g.63951366G>C	GRCh37
NC_000008.9:g.64113920G>C	NCBI36
NG_028126.1:g.5245C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000677327.1:n.601C>G
ENST00000677482.1:c.-39C>G	ENSP00000504590.1:n.-39C>G
ENST00000679326.1:c.-39C>G	ENSP00000504262.1:n.-39C>G
ENST00000260118.6:c.-39C>G	ENSP00000260118.6:n.-39C>G
NM_003878.2:c.-39C>G	NP_003869.1:n.-39C>G
XM_011517623.1:c.-39C>G	XP_011515925.1:n.-39C>G