Canonical Allele Identifier: CA99705333

Gene: ALB

Linked Data

• dbSNP Id: rs180747504
• gnomAD v2: 4-74278999-A-T
• gnomAD v3: 4-73413282-A-T
• gnomAD v4: 4-73413282-A-T
• MyVariant Identifiers: chr4:g.74278999A>T (hg19) ; chr4:g.73413282A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413282A>T , CM000666.2:g.73413282A>T	GRCh38
NC_000004.11:g.74278999A>T , CM000666.1:g.74278999A>T	GRCh37
NC_000004.10:g.74497863A>T	NCBI36
NG_009291.1:g.14028A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.844-138A>T MANE Select	ENSP00000295897.4:n.844-138A>T
ENST00000295897.8:c.844-138A>T	ENSP00000295897.4:n.844-138A>T
ENST00000401494.7:c.499-138A>T	ENSP00000384695.3:n.499-138A>T
ENST00000415165.6:c.268-138A>T	ENSP00000401820.2:n.268-138A>T
ENST00000476441.6:c.*123-138A>T	ENSP00000423727.1:n.*123-138A>T
ENST00000484992.1:n.26A>T
ENST00000503124.5:c.394-138A>T	ENSP00000421027.1:n.394-138A>T
ENST00000505649.5:n.530-138A>T
ENST00000509063.5:c.844-138A>T	ENSP00000422784.1:n.844-138A>T
ENST00000511370.1:c.377-138A>T
ENST00000621085.4:c.491-1824A>T	ENSP00000483421.1:n.491-1824A>T
ENST00000621628.4:c.487-1820A>T	ENSP00000480485.1:n.487-1820A>T
NM_000477.5:c.844-138A>T	NP_000468.1:n.844-138A>T
NM_000477.6:c.844-138A>T	NP_000468.1:n.844-138A>T
NM_000477.7:c.844-138A>T MANE Select	NP_000468.1:n.844-138A>T