Canonical Allele Identifier: CA552304200

Gene: ALB

Linked Data

• dbSNP Id: rs1156289309
• gnomAD v2: 4-74269964-G-T
• gnomAD v3: 4-73404247-G-T
• gnomAD v4: 4-73404247-G-T
• MyVariant Identifiers: chr4:g.74269964G>T (hg19) ; chr4:g.73404247G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404247G>T , CM000666.2:g.73404247G>T	GRCh38
NC_000004.11:g.74269964G>T , CM000666.1:g.74269964G>T	GRCh37
NC_000004.10:g.74488828G>T	NCBI36
NG_009291.1:g.4993G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.8:c.-81G>T	ENSP00000295897.4:n.-81G>T
ENST00000441319.5:c.48-122G>T	ENSP00000392541.1:n.48-122G>T
NM_000477.6:c.-81G>T	NP_000468.1:n.-81G>T