Canonical Allele Identifier: CA2670937833

Gene: ALB

Linked Data

• gnomAD v4: 4-73413284-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413284C>G , CM000666.2:g.73413284C>G	GRCh38
NC_000004.11:g.74279001C>G , CM000666.1:g.74279001C>G	GRCh37
NC_000004.10:g.74497865C>G	NCBI36
NG_009291.1:g.14030C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.844-136C>G MANE Select	ENSP00000295897.4:n.844-136C>G
ENST00000295897.8:c.844-136C>G	ENSP00000295897.4:n.844-136C>G
ENST00000401494.7:c.499-136C>G	ENSP00000384695.3:n.499-136C>G
ENST00000415165.6:c.268-136C>G	ENSP00000401820.2:n.268-136C>G
ENST00000476441.6:c.*123-136C>G	ENSP00000423727.1:n.*123-136C>G
ENST00000484992.1:n.28C>G
ENST00000503124.5:c.394-136C>G	ENSP00000421027.1:n.394-136C>G
ENST00000505649.5:n.530-136C>G
ENST00000509063.5:c.844-136C>G	ENSP00000422784.1:n.844-136C>G
ENST00000511370.1:c.377-136C>G
ENST00000621085.4:c.491-1822C>G	ENSP00000483421.1:n.491-1822C>G
ENST00000621628.4:c.487-1818C>G	ENSP00000480485.1:n.487-1818C>G
NM_000477.5:c.844-136C>G	NP_000468.1:n.844-136C>G
NM_000477.6:c.844-136C>G	NP_000468.1:n.844-136C>G
NM_000477.7:c.844-136C>G MANE Select	NP_000468.1:n.844-136C>G