Canonical Allele Identifier: CA99696081

Gene: ALB

Linked Data

• dbSNP Id: rs868248392
• MyVariant Identifiers: chr4:g.74269771T>C (hg19) ; chr4:g.73404054T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404054T>C , CM000666.2:g.73404054T>C	GRCh38
NC_000004.11:g.74269771T>C , CM000666.1:g.74269771T>C	GRCh37
NC_000004.10:g.74488635T>C	NCBI36
NG_009291.1:g.4800T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000441319.5:c.48-315T>C	ENSP00000392541.1:n.48-315T>C